Variant report

Variant rs58172099
Chromosome Location chr9:638588-638589
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:616800-655800 Weak transcription Pancreas Pancrea
2 chr9:621800-641800 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr9:626400-641400 Weak transcription Primary T cells from cord blood blood
4 chr9:628800-649400 Weak transcription Duodenum Mucosa Duodenum
5 chr9:632200-648600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:634400-648600 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr9:634400-649000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr9:634600-647600 Weak transcription A549 lung
9 chr9:634600-648800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr9:635000-639000 Weak transcription H1 Cell Line embryonic stem cell
11 chr9:635000-650400 Weak transcription Fetal Intestine Small intestine
12 chr9:635200-648600 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr9:635200-649800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:635400-649400 Weak transcription Right Atrium heart
15 chr9:635600-649600 Weak transcription Left Ventricle heart
16 chr9:637600-648400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr9:638000-639200 Enhancers Brain Anterior Caudate brain
18 chr9:638200-638600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
19 chr9:638200-638600 Enhancers Right Ventricle heart
20 chr9:638200-638800 Enhancers iPS-20b Cell Line embryonic stem cell
21 chr9:638200-639200 Enhancers Fetal Heart heart

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