Variant report

Variant rs2162217
Chromosome Location chr15:56620278-56620279
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:56613400-56623400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr15:56619400-56621400 Enhancers Placenta Placenta
3 chr15:56619600-56620400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr15:56619600-56620400 Flanking Active TSS NHEK skin
5 chr15:56619600-56620800 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr15:56619600-56621200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:56619800-56620400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr15:56619800-56620400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr15:56619800-56620400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr15:56619800-56620600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr15:56619800-56621200 Enhancers Esophagus oesophagus
12 chr15:56620000-56621200 Enhancers HMEC breast
13 chr15:56620200-56620400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr15:56620200-56620800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr15:56620200-56620800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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