Variant report

Variant rs4340077
Chromosome Location chr11:70890503-70890504
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:70858200-70891000 Weak transcription Gastric stomach
2 chr11:70882600-70892200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr11:70886600-70891000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr11:70887000-70891000 Weak transcription Pancreas Pancrea
5 chr11:70887200-70891000 Weak transcription H9 Cell Line embryonic stem cell
6 chr11:70887200-70892200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr11:70887200-70892400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr11:70887400-70890600 Weak transcription Fetal Intestine Small intestine
9 chr11:70889600-70891000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:70889600-70896000 Weak transcription Muscle Satellite Cultured Cells --
11 chr11:70890000-70891000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr11:70890200-70891400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:70890200-70892000 Enhancers Liver Liver
14 chr11:70890400-70893000 Enhancers HepG2 liver

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