UCSC Genome Browser on Human Dec. 2013 (GRCh38/hg38) Assembly
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chr1:9,428,538-15,815,791 6,387,254 bp.
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-   Mapping and Sequencing
Base Position
p12 Assembly
p12 Chromosome Band
p12 Gap
Short Match
-   Genes and Gene Predictions
Ribo-seq SmProt ATG
Ribo-seq SmProt non-ATG
Literature SmProt
Database SmProt
MS SmProt
p12 All GENCODE...
-   Phenotype and Literature
ClinVar variants
-   Comparative Genomics
-   Variation
Common SNPs(150)
All SNPs(150)
Flagged SNPs(150)
Mult. SNPs(150)
SmProt variants
gnomAD Variants...
NyuWa variants
-   Repeats
p12 RepeatMasker