Variant report

Variant rs12418368
Chromosome Location chr11:34050532-34050533
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34048800-34050600 Enhancers Fetal Intestine Small intestine
2 chr11:34048800-34052400 Enhancers Cortex derived primary cultured neurospheres brain
3 chr11:34049000-34050600 Enhancers Fetal Intestine Large intestine
4 chr11:34049000-34050600 Enhancers Rectal Mucosa Donor 31 rectum
5 chr11:34049200-34050600 Enhancers Placenta Placenta
6 chr11:34049200-34051600 Enhancers Stomach Mucosa stomach
7 chr11:34049400-34052400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr11:34049600-34050800 Weak transcription Aorta Aorta
9 chr11:34049600-34051200 Enhancers Fetal Brain Male brain
10 chr11:34050000-34050600 Enhancers Esophagus oesophagus
11 chr11:34050000-34052600 Enhancers NHEK skin
12 chr11:34050200-34051400 Weak transcription Duodenum Mucosa Duodenum
13 chr11:34050200-34051800 Weak transcription Colonic Mucosa Colon
14 chr11:34050200-34052000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr11:34050200-34052000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr11:34050400-34051000 Enhancers HepG2 liver
17 chr11:34050400-34051200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr11:34050400-34051400 Weak transcription Breast Myoepithelial Primary Cells Breast
19 chr11:34050400-34055800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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