Variant report

Variant rs28661391
Chromosome Location chr8:11807797-11807798
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11806600-11809000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr8:11807200-11807800 Bivalent Enhancer Placenta Amnion Placenta Amnion
3 chr8:11807200-11808800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr8:11807600-11807800 Bivalent Enhancer Placenta Placenta
5 chr8:11807600-11808800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr8:11807600-11812200 Weak transcription Fetal Heart heart
7 chr8:11807600-11812600 Weak transcription Right Atrium heart

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