Variant report

Variant rs7030823
Chromosome Location chr9:139848717-139848718
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139845000-139853600 Weak transcription Placenta Amnion Placenta Amnion
2 chr9:139845200-139860200 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr9:139845200-139860400 Weak transcription Right Atrium heart
4 chr9:139845400-139849200 Weak transcription Primary T helper 17 cells PMA-I stimulated --
5 chr9:139845400-139852800 Weak transcription Thymus Thymus
6 chr9:139845400-139853000 Weak transcription Primary mononuclear cells fromperipheralblood Blood
7 chr9:139845400-139855400 Weak transcription Gastric stomach
8 chr9:139845400-139860200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr9:139845600-139849400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr9:139845600-139854000 Weak transcription Pancreas Pancrea
11 chr9:139846200-139852600 Weak transcription Primary T helper cells PMA-I stimulated --
12 chr9:139846200-139860200 Weak transcription Liver Liver
13 chr9:139846600-139852000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
14 chr9:139847000-139851000 Strong transcription Fetal Intestine Small intestine
15 chr9:139847200-139853400 Weak transcription Spleen Spleen
16 chr9:139847600-139849400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr9:139847800-139855600 Weak transcription Right Ventricle heart
18 chr9:139848200-139849400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
19 chr9:139848200-139857400 Weak transcription Fetal Heart heart
20 chr9:139848400-139848800 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
21 chr9:139848400-139849800 Weak transcription Fetal Adrenal Gland Adrenal Gland
22 chr9:139848600-139850800 Weak transcription Fetal Intestine Large intestine

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