Variant report

Variant rs4302194
Chromosome Location chr2:11490158-11490159
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:11485800-11497400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr2:11485800-11497400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:11486200-11493800 Weak transcription Stomach Mucosa stomach
4 chr2:11486400-11490400 Enhancers HepG2 liver
5 chr2:11486600-11493000 Weak transcription Lung lung
6 chr2:11488400-11490200 Enhancers Cortex derived primary cultured neurospheres brain
7 chr2:11488600-11490200 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr2:11488800-11494000 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr2:11489000-11492600 Weak transcription Fetal Intestine Large intestine
10 chr2:11489000-11492600 Weak transcription Placenta Placenta
11 chr2:11489000-11495600 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr2:11489200-11492600 Weak transcription Liver Liver
13 chr2:11489400-11492800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:11489400-11493400 Weak transcription Gastric stomach
15 chr2:11489400-11494600 Weak transcription Fetal Intestine Small intestine
16 chr2:11489400-11496800 Weak transcription Adipose Nuclei Adipose

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