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Configure Tracks on UCSC Genome Browser: Human Dec. 2013 (GRCh38/hg38) (hg38_2)
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-   Variation    
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
-   Mapping and Sequencing    
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 ()
-   Genes and Gene Predictions    
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)
-   Phenotype and Literature    
ClinVar Variants ClinVar Variants
-   Comparative Genomics    
Conservation Vertebrate Multiz Alignment & Conservation (100 Species)
-   Repeats    
p12 RepeatMasker Repeating Elements by RepeatMasker