Variant report

Variant rs192924619
Chromosome Location chr1:153402055-153402056
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153401400-153403400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:153401600-153402200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:153401800-153402800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:153401800-153403000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:153402000-153402600 Enhancers NHEK skin
6 chr1:153402000-153403800 Enhancers Esophagus oesophagus

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