Variant report

Variant rs12002163
Chromosome Location chr9:503175-503176
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:489600-503200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr9:495800-503200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr9:496200-503200 Weak transcription Gastric stomach
4 chr9:496200-503200 Weak transcription A549 lung
5 chr9:497400-503400 Weak transcription Pancreas Pancrea
6 chr9:502000-503200 Weak transcription Fetal Intestine Small intestine
7 chr9:502600-503400 Weak transcription H9 Cell Line embryonic stem cell
8 chr9:502800-503200 Enhancers Primary T helper cells PMA-I stimulated --
9 chr9:502800-503200 Enhancers Rectal Mucosa Donor 31 rectum
10 chr9:502800-503800 Enhancers Stomach Mucosa stomach
11 chr9:503000-503200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr9:503000-503200 Enhancers Duodenum Mucosa Duodenum
13 chr9:503000-503200 Bivalent Enhancer Fetal Intestine Large intestine
14 chr9:503000-503400 Enhancers Primary T helper cells fromperipheralblood blood
15 chr9:503000-503400 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr9:503000-503600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
17 chr9:503000-504200 Flanking Active TSS Fetal Heart heart

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