Variant report

Variant rs377739490
Chromosome Location chr14:104577854-104577855
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104566200-104582600 Weak transcription Right Atrium heart
2 chr14:104570400-104582400 Weak transcription Ovary ovary
3 chr14:104575000-104582200 Weak transcription HMEC breast
4 chr14:104575400-104578600 Weak transcription NHEK skin
5 chr14:104575600-104580200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:104575800-104579000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr14:104576000-104580200 Enhancers Placenta Placenta
8 chr14:104577400-104581600 Enhancers Esophagus oesophagus
9 chr14:104577600-104578400 Weak transcription H9 Cell Line embryonic stem cell
10 chr14:104577600-104578800 Bivalent Enhancer Colonic Mucosa Colon
11 chr14:104577600-104580400 Enhancers Stomach Mucosa stomach
12 chr14:104577600-104582200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr14:104577600-104582200 Weak transcription Placenta Amnion Placenta Amnion
14 chr14:104577800-104578000 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
15 chr14:104577800-104578600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr14:104577800-104578800 Weak transcription Liver Liver
17 chr14:104577800-104579200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr14:104577800-104580400 Enhancers Gastric stomach

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