Variant report

Variant rs139249150
Chromosome Location chr9:12685363-12685364
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:12680200-12688200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr9:12683600-12685600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr9:12684200-12685600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr9:12684200-12686000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr9:12684400-12686000 Enhancers HUVEC blood vessel
6 chr9:12684800-12685400 Enhancers Placenta Amnion Placenta Amnion
7 chr9:12684800-12685400 Enhancers NHEK skin
8 chr9:12684800-12685600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr9:12684800-12685600 Enhancers NH-A brain
10 chr9:12685000-12685400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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