Variant report

Variant rs12379956
Chromosome Location chr9:110899161-110899162
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110868600-110899800 Weak transcription H9 Cell Line embryonic stem cell
2 chr9:110882000-110904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:110896000-110899800 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr9:110896200-110899800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr9:110896200-110900200 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr9:110896400-110904400 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr9:110896400-110905000 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr9:110896600-110904600 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr9:110897000-110904400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:110898000-110904200 Weak transcription Stomach Mucosa stomach
11 chr9:110899000-110899800 Weak transcription Fetal Brain Male brain
12 chr9:110899000-110900000 Enhancers Skeletal Muscle Male skeletal muscle
13 chr9:110899000-110901000 Enhancers Skeletal Muscle Female skeletal muscle
14 chr9:110899000-110904400 Weak transcription Esophagus oesophagus

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