UCSC Genome Browser on Human Dec. 2013 (GRCh38/hg38) Assembly (hg38_2)
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chr22:42,126,499-42,130,810 4,312 bp.
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-   Variation
NyuWa variants
1000G Ph3 Vars
Common SNPs(150)
All SNPs(150)
Flagged SNPs(150)
Mult. SNPs(150)
gnomAD Variants...
Blocks_chr22
Recombination Map
-   Mapping and Sequencing
Base Position
p12 Assembly
p12 Chromosome Band
p12 Gap
Short Match
-   Genes and Gene Predictions
updated NCBI RefSeq
p12 updated All GENCODE...
-   Phenotype and Literature
ClinVar Variants
-   Comparative Genomics
Conservation
-   Repeats
p12 RepeatMasker