Variant report

Variant rs7875960
Chromosome Location chr9:141044168-141044169
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140988200-141044600 Weak transcription Right Atrium heart
2 chr9:141042400-141044200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:141042400-141044600 Weak transcription K562 blood
4 chr9:141042600-141044200 Weak transcription Placenta Placenta
5 chr9:141042600-141044400 Weak transcription HepG2 liver
6 chr9:141042600-141044600 Weak transcription Adipose Nuclei Adipose
7 chr9:141042600-141044600 Weak transcription Ovary ovary
8 chr9:141043800-141044400 Enhancers Primary T cells from cord blood blood
9 chr9:141044000-141044400 Bivalent Enhancer Primary B cells from peripheral blood blood

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