Variant report

Variant rs2987081
Chromosome Location chr9:16012046-16012047
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16002400-16012800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:16010400-16013400 Enhancers Osteobl bone
3 chr9:16011000-16014000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:16011800-16013000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr9:16011800-16013200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr9:16011800-16013200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:16011800-16013200 Enhancers NHDF-Ad bronchial
8 chr9:16012000-16013400 Enhancers Muscle Satellite Cultured Cells --
9 chr9:16012000-16013600 Enhancers NH-A brain

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