Variant report

Variant rs4280634
Chromosome Location chr3:133825328-133825329
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:133821000-133826400 Weak transcription Right Atrium heart
2 chr3:133823200-133825400 Weak transcription HUVEC blood vessel
3 chr3:133823400-133826600 ZNF genes & repeats Aorta Aorta
4 chr3:133823400-133830800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr3:133824200-133827000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr3:133824600-133825800 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr3:133824600-133827600 Enhancers Pancreas Pancrea
8 chr3:133824800-133825400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
9 chr3:133824800-133826000 Enhancers HepG2 liver
10 chr3:133825000-133825400 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr3:133825000-133826000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr3:133825000-133826000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr3:133825200-133825800 Enhancers GM12878-XiMat blood
14 chr3:133825200-133827600 Enhancers Fetal Intestine Small intestine

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