Variant report

Variant rs17864705
Chromosome Location chr2:234672328-234672329
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234666800-234673600 Weak transcription Colonic Mucosa Colon
2 chr2:234667200-234672400 Weak transcription Rectal Mucosa Donor 29 rectum
3 chr2:234667200-234673800 Enhancers Stomach Mucosa stomach
4 chr2:234669200-234683800 Weak transcription Gastric stomach
5 chr2:234669800-234673200 Active TSS Liver Liver
6 chr2:234670200-234673000 Weak transcription Esophagus oesophagus
7 chr2:234670600-234672400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr2:234670600-234672400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:234670600-234672800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr2:234670800-234672400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:234671000-234672400 Weak transcription HMEC breast
12 chr2:234671000-234672400 Weak transcription NHEK skin
13 chr2:234671000-234672600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:234671400-234675200 Enhancers Fetal Intestine Small intestine
15 chr2:234671600-234672800 Enhancers Rectal Mucosa Donor 31 rectum
16 chr2:234672000-234673600 Active TSS Duodenum Mucosa Duodenum
17 chr2:234672000-234673800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr2:234672000-234673800 Enhancers A549 lung
19 chr2:234672000-234675200 Enhancers Fetal Intestine Large intestine
20 chr2:234672200-234673000 Enhancers Small Intestine intestine
21 chr2:234672200-234673200 Enhancers Osteobl bone

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