Variant report

Variant rs726966
Chromosome Location chr6:15894027-15894028
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15883400-15895800 Weak transcription Esophagus oesophagus
2 chr6:15889600-15897200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:15889600-15897400 Weak transcription Spleen Spleen
4 chr6:15889800-15895800 Weak transcription Fetal Lung lung
5 chr6:15890200-15897200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:15892800-15894400 Weak transcription Placenta Placenta
7 chr6:15893000-15897200 Weak transcription Right Atrium heart
8 chr6:15893400-15896800 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr6:15893600-15897000 Weak transcription Primary monocytes fromperipheralblood blood
10 chr6:15894000-15894200 Flanking Active TSS HUES48 Cell Line embryonic stem cell
11 chr6:15894000-15895400 Enhancers iPS-15b Cell Line embryonic stem cell

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