Variant report

Variant rs4880182
Chromosome Location chr9:139883413-139883414
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139873600-139886200 Weak transcription Pancreas Pancrea
2 chr9:139879800-139884200 Weak transcription Hela-S3 cervix
3 chr9:139880000-139885400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
4 chr9:139880600-139886000 Weak transcription Primary T killer naive cells fromperipheralblood blood
5 chr9:139882000-139884800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr9:139882400-139883800 Bivalent Enhancer HepG2 liver
7 chr9:139883000-139883600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr9:139883000-139886400 Weak transcription Small Intestine intestine
9 chr9:139883000-139887000 Enhancers Placenta Placenta
10 chr9:139883200-139884400 Enhancers K562 blood

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