Variant report

Variant rs74047259
Chromosome Location chr14:37711142-37711143
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37694800-37756400 Weak transcription Aorta Aorta
2 chr14:37696000-37715400 Weak transcription Fetal Intestine Small intestine
3 chr14:37702400-37717000 Weak transcription HUVEC blood vessel
4 chr14:37706400-37717000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr14:37706400-37717400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr14:37706400-37723200 Weak transcription NHEK skin
7 chr14:37707200-37717200 Weak transcription Ovary ovary
8 chr14:37710400-37715800 Weak transcription Stomach Mucosa stomach
9 chr14:37710400-37724000 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr14:37710600-37722000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr14:37710600-37723800 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr14:37710800-37721200 Weak transcription H1 Cell Line embryonic stem cell

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