Variant report

Variant rs7860430
Chromosome Location chr9:139884447-139884448
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139873600-139886200 Weak transcription Pancreas Pancrea
2 chr9:139880000-139885400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
3 chr9:139880600-139886000 Weak transcription Primary T killer naive cells fromperipheralblood blood
4 chr9:139882000-139884800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr9:139883000-139886400 Weak transcription Small Intestine intestine
6 chr9:139883000-139887000 Enhancers Placenta Placenta
7 chr9:139883800-139886400 Enhancers HepG2 liver
8 chr9:139884200-139884800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr9:139884200-139885000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr9:139884200-139885400 Enhancers Hela-S3 cervix
11 chr9:139884400-139884800 Weak transcription K562 blood

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