Variant report

Variant rs9638741
Chromosome Location chr7:17419519-17419520
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr7:17412400-17420200 Weak transcription NHLF lung
4 chr7:17412600-17420000 Weak transcription Fetal Intestine Large intestine
5 chr7:17412600-17420400 Weak transcription Osteobl bone
6 chr7:17412600-17420600 Weak transcription Pancreas Pancrea
7 chr7:17412600-17421200 Weak transcription NHEK skin
8 chr7:17413200-17420000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:17414600-17420000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr7:17414800-17424200 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr7:17415000-17420000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr7:17416400-17420000 Weak transcription Liver Liver
13 chr7:17417400-17420600 Enhancers Duodenum Mucosa Duodenum
14 chr7:17418000-17420000 Weak transcription Fetal Intestine Small intestine
15 chr7:17418800-17421000 Enhancers Stomach Mucosa stomach
16 chr7:17419400-17421600 Enhancers NHDF-Ad bronchial

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