Variant report

Variant rs116897693
Chromosome Location chr17:43780887-43780888
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr17:43780400-43781600 Enhancers iPS-15b Cell Line embryonic stem cell
3 chr17:43780400-43783400 Enhancers A549 lung
4 chr17:43780400-43783600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr17:43780600-43781200 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr17:43780600-43781200 Enhancers H1 Cell Line embryonic stem cell
7 chr17:43780600-43781200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
8 chr17:43780800-43781000 Flanking Bivalent TSS/Enh H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr17:43780800-43781000 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
10 chr17:43780800-43781000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr17:43780800-43781000 Enhancers Esophagus oesophagus
12 chr17:43780800-43781200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr17:43780800-43781200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr17:43780800-43781200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
15 chr17:43780800-43784000 Enhancers HMEC breast

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