Variant report

Variant rs12002249
Chromosome Location chr9:637391-637392
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr9:628400-638200 Weak transcription Right Ventricle heart
5 chr9:628800-649400 Weak transcription Duodenum Mucosa Duodenum
6 chr9:632200-638200 Weak transcription Fetal Heart heart
7 chr9:632200-648600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr9:634400-648600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr9:634400-649000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr9:634600-647600 Weak transcription A549 lung
11 chr9:634600-648800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr9:635000-639000 Weak transcription H1 Cell Line embryonic stem cell
13 chr9:635000-650400 Weak transcription Fetal Intestine Small intestine
14 chr9:635200-648600 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr9:635200-649800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr9:635400-649400 Weak transcription Right Atrium heart
17 chr9:635600-649600 Weak transcription Left Ventricle heart
18 chr9:635800-637600 Genic enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr9:636800-637600 Enhancers Brain Inferior Temporal Lobe brain

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