Control track and group visibility more selectively below.
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Base Position |
| Chromosome position in bases. (Clicks here zoom in 3x) |
NyuWa variants |
| variants derived from NyuWa project |
1000G Ph3 Vars |
| 1000 Genomes Phase 3 Integrated Variant Calls from IGSR: SNVs and Indels |
Common SNPs(150) |
| Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples |
All SNPs(150) |
| Simple Nucleotide Polymorphisms (dbSNP 150) |
Flagged SNPs(150) |
| Simple Nucleotide Polymorphisms (dbSNP 150) Flagged by dbSNP as Clinically Assoc |
Mult. SNPs(150) |
| Simple Nucleotide Polymorphisms (dbSNP 150) That Map to Multiple Genomic Loci |
gnomAD Variants... |
| Genome Aggregation Database (gnomAD) Genome and Exome Variants |
gnomAD v3 |
| Genome Aggregation Database (gnomAD) Genome Variants v3 |
Blocks_chr22 |
| blocks of chr22 |
Recombination Map |
| Recombination map of 200 individuals |
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p12
Assembly |
| Assembly from Fragments |
p12
Chromosome Band |
| Chromosome Bands Localized by FISH Mapping Clones |
p12
Gap |
| Gap Locations |
Short Match |
| Perfect Matches to Short Sequence () |
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updated
NCBI RefSeq |
| RefSeq gene predictions from NCBI |
p12
updated
All GENCODE... |
| All GENCODE transcripts, including comprehensive set and previous version |
All GENCODE V31 |
| All GENCODE annotations from V31 (Ensembl 97) |
All GENCODE V28 |
| All GENCODE annotations from V28 (Ensembl 92) |
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ClinVar Variants |
| ClinVar Variants |
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Conservation |
| Vertebrate Multiz Alignment & Conservation (100 Species) |
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p12
RepeatMasker |
| Repeating Elements by RepeatMasker |
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