Variant report

Variant rs7416452
Chromosome Location chr1:172967538-172967539
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172960600-172974000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:172967000-172968200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:172967200-172968000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr1:172967200-172968000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:172967200-172968000 Enhancers NHEK skin
6 chr1:172967200-172968800 Enhancers HMEC breast
7 chr1:172967400-172967600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:172967400-172967800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:172967400-172968000 Enhancers HSMM muscle
10 chr1:172967400-172968200 Enhancers HSMMtube muscle

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