Variant report

Variant rs10233705
Chromosome Location chr7:17416616-17416617
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17412000-17418800 Weak transcription Stomach Mucosa stomach
2 chr7:17412000-17419000 Weak transcription Small Intestine intestine
3 chr7:17412200-17420600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17412200-17420600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr7:17412400-17420200 Weak transcription NHLF lung
6 chr7:17412600-17417400 Weak transcription Duodenum Mucosa Duodenum
7 chr7:17412600-17417600 Weak transcription Fetal Intestine Small intestine
8 chr7:17412600-17420000 Weak transcription Fetal Intestine Large intestine
9 chr7:17412600-17420400 Weak transcription Osteobl bone
10 chr7:17412600-17420600 Weak transcription Pancreas Pancrea
11 chr7:17412600-17421200 Weak transcription NHEK skin
12 chr7:17412800-17419400 Weak transcription NHDF-Ad bronchial
13 chr7:17413200-17420000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr7:17414600-17420000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:17414800-17424200 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr7:17415000-17420000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr7:17416400-17420000 Weak transcription Liver Liver

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