Variant report

Variant rs6906462
Chromosome Location chr6:26755600-26755601
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26747600-26757400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:26753000-26756000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:26755400-26755600 Enhancers K562 blood
4 chr6:26755600-26755800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr6:26755600-26755800 Bivalent Enhancer NHEK skin
6 chr6:26755600-26756000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
7 chr6:26755600-26756600 Flanking Active TSS K562 blood
8 chr6:26755600-26756800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin

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