Variant report

Variant rs9655142
Chromosome Location chr7:17415828-17415829
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr7:17412200-17416200 Weak transcription HSMMtube muscle
4 chr7:17412200-17420600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:17412200-17420600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr7:17412400-17420200 Weak transcription NHLF lung
7 chr7:17412600-17417400 Weak transcription Duodenum Mucosa Duodenum
8 chr7:17412600-17417600 Weak transcription Fetal Intestine Small intestine
9 chr7:17412600-17420000 Weak transcription Fetal Intestine Large intestine
10 chr7:17412600-17420400 Weak transcription Osteobl bone
11 chr7:17412600-17420600 Weak transcription Pancreas Pancrea
12 chr7:17412600-17421200 Weak transcription NHEK skin
13 chr7:17412800-17419400 Weak transcription NHDF-Ad bronchial
14 chr7:17413200-17420000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr7:17414600-17420000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:17414800-17424200 Weak transcription ES-I3 Cell Line embryonic stem cell
17 chr7:17415000-17420000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr7:17415800-17416400 Enhancers Liver Liver

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