Variant report

Variant rs1157906
Chromosome Location chr7:17531955-17531956
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17499400-17544600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:17528200-17532800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr7:17528400-17533200 Enhancers Primary T cells from cord blood blood
4 chr7:17529200-17535800 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr7:17530200-17532000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:17531800-17532000 Enhancers NHEK skin
7 chr7:17531800-17532400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr7:17531800-17532600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:17531800-17532600 Enhancers GM12878-XiMat blood
10 chr7:17531800-17532800 Enhancers HMEC breast

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