Variant report

Variant rs10276661
Chromosome Location chr7:17420241-17420242
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17412200-17420600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:17412200-17420600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr7:17412600-17420400 Weak transcription Osteobl bone
4 chr7:17412600-17420600 Weak transcription Pancreas Pancrea
5 chr7:17412600-17421200 Weak transcription NHEK skin
6 chr7:17414800-17424200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr7:17417400-17420600 Enhancers Duodenum Mucosa Duodenum
8 chr7:17418800-17421000 Enhancers Stomach Mucosa stomach
9 chr7:17419400-17421600 Enhancers NHDF-Ad bronchial
10 chr7:17420000-17420600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr7:17420000-17421000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr7:17420000-17421000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:17420000-17421200 Enhancers Liver Liver
14 chr7:17420000-17421200 Enhancers Fetal Intestine Large intestine
15 chr7:17420000-17421600 Enhancers Fetal Intestine Small intestine
16 chr7:17420000-17422200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr7:17420200-17420800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr7:17420200-17420800 Enhancers NHLF lung

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