Variant report

Variant rs553735148
Chromosome Location chr5:68135308-68135309
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:68133000-68142800 Weak transcription Aorta Aorta
2 chr5:68133600-68136800 Enhancers Placenta Amnion Placenta Amnion
3 chr5:68134000-68135600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr5:68134000-68135600 Enhancers NHDF-Ad bronchial
5 chr5:68134200-68135400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr5:68134200-68135400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr5:68134200-68135400 Enhancers Placenta Placenta
8 chr5:68134200-68135400 Enhancers HMEC breast
9 chr5:68134200-68135600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr5:68134200-68135800 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr5:68134800-68135400 Enhancers NHEK skin
12 chr5:68134800-68135800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr5:68134800-68136000 Enhancers Primary neutrophils fromperipheralblood blood
14 chr5:68135200-68135400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr5:68135200-68135600 Enhancers Adipose Nuclei Adipose
16 chr5:68135200-68139200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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