Variant report

Variant rs28608975
Chromosome Location chr9:71718348-71718349
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr9:71713200-71719600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr9:71714800-71719400 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr9:71715000-71719000 Weak transcription Gastric stomach
9 chr9:71715000-71735000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr9:71717400-71719000 Enhancers HepG2 liver
11 chr9:71717600-71719600 Enhancers Rectal Mucosa Donor 29 rectum
12 chr9:71718000-71718600 Enhancers Stomach Mucosa stomach
13 chr9:71718200-71718400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr9:71718200-71718400 Enhancers Pancreas Pancrea
15 chr9:71718200-71718600 Enhancers H1 Cell Line embryonic stem cell
16 chr9:71718200-71718600 Enhancers HUES6 Cell Line embryonic stem cell
17 chr9:71718200-71720200 Enhancers Liver Liver
18 chr9:71718200-71721000 Enhancers Fetal Intestine Large intestine
19 chr9:71718200-71721400 Enhancers Fetal Intestine Small intestine

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