Variant report

Variant rs184763486
Chromosome Location chr14:104327095-104327096
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104315200-104327600 Weak transcription Ovary ovary
2 chr14:104322600-104327800 Weak transcription Fetal Heart heart
3 chr14:104322800-104327800 Weak transcription Duodenum Mucosa Duodenum
4 chr14:104322800-104327800 Weak transcription Gastric stomach
5 chr14:104323600-104327800 Weak transcription Pancreas Pancrea
6 chr14:104323600-104336000 Weak transcription Placenta Amnion Placenta Amnion
7 chr14:104323600-104337600 Weak transcription Fetal Intestine Small intestine
8 chr14:104325200-104333600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr14:104325800-104329000 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr14:104326000-104327200 Enhancers Liver Liver
11 chr14:104326400-104327800 Weak transcription Lung lung
12 chr14:104326400-104327800 Weak transcription Spleen Spleen
13 chr14:104326400-104328200 Enhancers Placenta Placenta
14 chr14:104326600-104327800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr14:104326600-104327800 Weak transcription Fetal Muscle Leg muscle
16 chr14:104326600-104328000 Weak transcription Left Ventricle heart
17 chr14:104326600-104332200 Weak transcription Right Ventricle heart
18 chr14:104326600-104336400 Weak transcription Right Atrium heart
19 chr14:104326800-104327800 Enhancers HepG2 liver

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