Variant report

Variant rs13015969
Chromosome Location chr2:114749798-114749799
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114734000-114751800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr2:114734400-114749800 Weak transcription Primary T cells fromperipheralblood blood
3 chr2:114736200-114761000 Weak transcription HSMMtube muscle
4 chr2:114737600-114751400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr2:114737800-114754400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr2:114739600-114752600 Weak transcription NH-A brain
7 chr2:114741200-114761000 Weak transcription HSMM muscle
8 chr2:114743000-114751000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:114746200-114752800 Weak transcription HepG2 liver
10 chr2:114749000-114749800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:114749400-114750000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links