Variant report

Variant rs62056881
Chromosome Location chr17:43782455-43782456
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43778400-43782600 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr17:43780400-43783400 Enhancers A549 lung
3 chr17:43780400-43783600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr17:43780800-43784000 Enhancers HMEC breast
5 chr17:43781000-43782800 Weak transcription Esophagus oesophagus
6 chr17:43781200-43782600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr17:43781200-43786200 Weak transcription H1 Cell Line embryonic stem cell
8 chr17:43781200-43786200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr17:43781600-43786800 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr17:43782200-43782800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr17:43782200-43783400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr17:43782400-43782600 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr17:43782400-43782800 Bivalent Enhancer HepG2 liver
14 chr17:43782400-43783000 Enhancers Stomach Mucosa stomach
15 chr17:43782400-43783400 Enhancers NH-A brain
16 chr17:43782400-43783600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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