Variant report

Variant rs11186078
Chromosome Location chr10:91983241-91983242
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:91978000-91986200 Weak transcription Aorta Aorta
2 chr10:91980000-91984800 Weak transcription Placenta Amnion Placenta Amnion
3 chr10:91981400-91983400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr10:91981400-91984000 Enhancers NHEK skin
5 chr10:91981800-91984200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr10:91982000-91983400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr10:91982000-91984000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr10:91982800-91984200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr10:91982800-91984600 Enhancers HMEC breast
10 chr10:91983000-91985600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr10:91983000-91986000 Weak transcription NH-A brain
12 chr10:91983000-91986400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr10:91983200-91986000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr10:91983200-91986200 Weak transcription HUVEC blood vessel
15 chr10:91983200-91986800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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