Variant report

Variant rs11770368
Chromosome Location chr7:17713605-17713606
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17702800-17713800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:17712600-17715400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr7:17713000-17722000 Enhancers HMEC breast
4 chr7:17713200-17716000 Enhancers NHEK skin
5 chr7:17713400-17713800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr7:17713400-17715200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr7:17713400-17715200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:17713400-17715200 Enhancers Placenta Placenta
9 chr7:17713600-17714000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr7:17713600-17714600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr7:17713600-17715000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr7:17713600-17715800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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