Variant report

Variant rs471145
Chromosome Location chr6:128981829-128981830
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:128977400-128982000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr6:128980600-128982000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:128980600-128982000 Enhancers HMEC breast
4 chr6:128981000-128982000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr6:128981000-128982200 Flanking Active TSS NHEK skin
6 chr6:128981200-128982000 Weak transcription Fetal Thymus thymus
7 chr6:128981600-128985400 Weak transcription Fetal Heart heart
8 chr6:128981800-128982000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr6:128981800-128982200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin

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