Variant report

Variant rs12343257
Chromosome Location chr9:71718136-71718137
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:71701800-71735200 Weak transcription Primary T cells from cord blood blood
2 chr9:71706200-71720200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:71710200-71719400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr9:71712600-71735200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr9:71713000-71720200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:71713200-71718200 Weak transcription Liver Liver
7 chr9:71713200-71719600 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr9:71714800-71718200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr9:71714800-71719400 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr9:71715000-71718200 Weak transcription Fetal Intestine Small intestine
11 chr9:71715000-71719000 Weak transcription Gastric stomach
12 chr9:71715000-71735000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr9:71715400-71718200 Weak transcription Fetal Intestine Large intestine
14 chr9:71717400-71719000 Enhancers HepG2 liver
15 chr9:71717600-71719600 Enhancers Rectal Mucosa Donor 29 rectum
16 chr9:71718000-71718600 Enhancers Stomach Mucosa stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links