Variant report

Variant rs16930376
Chromosome Location chr12:26399829-26399830
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:26393000-26400200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr12:26393000-26400400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr12:26394000-26404600 Weak transcription Pancreas Pancrea
4 chr12:26395600-26400400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:26396000-26401000 Enhancers Stomach Mucosa stomach
6 chr12:26397000-26401000 Enhancers HMEC breast
7 chr12:26397600-26400400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:26397800-26400400 Enhancers Rectal Mucosa Donor 29 rectum
9 chr12:26397800-26401200 Enhancers Rectal Mucosa Donor 31 rectum
10 chr12:26398000-26400400 Enhancers NHEK skin
11 chr12:26398200-26400000 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr12:26398200-26400000 Enhancers Duodenum Mucosa Duodenum
13 chr12:26398400-26400000 Enhancers Fetal Intestine Large intestine
14 chr12:26398600-26400400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr12:26398800-26400000 Enhancers Hela-S3 cervix
16 chr12:26399000-26400400 Enhancers Esophagus oesophagus
17 chr12:26399000-26400600 Enhancers Gastric stomach
18 chr12:26399200-26400200 Weak transcription Sigmoid Colon Sigmoid Colon
19 chr12:26399200-26400800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
20 chr12:26399200-26400800 Weak transcription Small Intestine intestine
21 chr12:26399800-26400800 Weak transcription Fetal Intestine Small intestine
22 chr12:26399800-26402200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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