Variant report

Variant rs56894679
Chromosome Location chr7:17647477-17647478
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17641600-17663000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:17642400-17657400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:17643200-17647600 Weak transcription HMEC breast
4 chr7:17646200-17648800 Enhancers Hela-S3 cervix
5 chr7:17646600-17648800 Enhancers NHDF-Ad bronchial
6 chr7:17647400-17648000 Weak transcription Fetal Intestine Large intestine
7 chr7:17647400-17648600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr7:17647400-17648600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:17647400-17648800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr7:17647400-17648800 Enhancers Muscle Satellite Cultured Cells --
11 chr7:17647400-17648800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr7:17647400-17648800 Enhancers HSMM muscle
13 chr7:17647400-17649200 Enhancers Monocytes-CD14+_RO01746 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links