Variant report

Variant rs4941661
Chromosome Location chr13:50431366-50431367
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50422200-50431400 Weak transcription Pancreas Pancrea
2 chr13:50422200-50436600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr13:50422600-50431400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr13:50430200-50431400 Enhancers HepG2 liver
5 chr13:50431000-50431400 Enhancers A549 lung
6 chr13:50431000-50433000 Enhancers Muscle Satellite Cultured Cells --
7 chr13:50431200-50431400 Enhancers Liver Liver
8 chr13:50431200-50432400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr13:50431200-50433800 Enhancers NHLF lung
10 chr13:50431200-50434600 Enhancers HMEC breast

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