Variant report

Variant rs2655872
Chromosome Location chr12:60788564-60788565
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:60785200-60788800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:60787800-60789400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr12:60787800-60789800 Enhancers Hela-S3 cervix
4 chr12:60788000-60788600 Enhancers NH-A brain
5 chr12:60788000-60789000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr12:60788000-60789200 Enhancers NHDF-Ad bronchial
7 chr12:60788000-60789600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr12:60788000-60789600 Enhancers HMEC breast
9 chr12:60788000-60789800 Enhancers NHEK skin
10 chr12:60788200-60789000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr12:60788200-60789800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr12:60788400-60789400 Enhancers HUVEC blood vessel
13 chr12:60788400-60789600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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