Variant report

Variant rs539311569
Chromosome Location chr4:3782961-3782962
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3780400-3783000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr4:3781800-3783000 Flanking Active TSS HepG2 liver
3 chr4:3782000-3783000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:3782000-3783000 Enhancers Placenta Amnion Placenta Amnion
5 chr4:3782000-3783000 Enhancers K562 blood
6 chr4:3782200-3783000 Enhancers H1 Cell Line embryonic stem cell
7 chr4:3782200-3784800 Bivalent Enhancer Placenta Placenta
8 chr4:3782400-3783000 Enhancers A549 lung
9 chr4:3782600-3783000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr4:3782600-3784000 ZNF genes & repeats Fetal Intestine Large intestine
11 chr4:3782600-3786400 Weak transcription Hela-S3 cervix
12 chr4:3782800-3783000 Weak transcription Fetal Intestine Small intestine

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