Variant report

Variant rs58160764
Chromosome Location chr1:79153828-79153829
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:79151200-79156400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:79152600-79154600 Enhancers Liver Liver
3 chr1:79152800-79159000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:79153000-79155000 Enhancers Fetal Brain Male brain
5 chr1:79153000-79155000 Enhancers HSMM muscle
6 chr1:79153000-79155200 Enhancers Osteobl bone
7 chr1:79153000-79159000 Enhancers NHDF-Ad bronchial
8 chr1:79153200-79154200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:79153200-79158800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr1:79153400-79154000 Enhancers HUVEC blood vessel
11 chr1:79153400-79154400 Flanking Active TSS Muscle Satellite Cultured Cells --
12 chr1:79153400-79154400 Enhancers HMEC breast
13 chr1:79153400-79154400 Enhancers NHLF lung
14 chr1:79153400-79154600 Enhancers NH-A brain
15 chr1:79153400-79155000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr1:79153400-79155000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr1:79153600-79154400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
18 chr1:79153800-79154400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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