Variant report

Variant rs74101688
Chromosome Location chr1:94212527-94212528
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94199400-94217400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94206000-94212600 Weak transcription HMEC breast
3 chr1:94208200-94215600 Weak transcription Aorta Aorta
4 chr1:94209400-94212600 Enhancers NHEK skin
5 chr1:94209800-94212600 Enhancers Fetal Thymus thymus
6 chr1:94210200-94212600 Enhancers Esophagus oesophagus
7 chr1:94210800-94215600 Weak transcription Thymus Thymus
8 chr1:94211800-94215600 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr1:94212400-94212600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
10 chr1:94212400-94212600 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr1:94212400-94213200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:94212400-94213200 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:94212400-94214400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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