Variant report

Variant rs34281542
Chromosome Location chr2:67615604-67615605
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:67601800-67616200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr2:67602200-67615800 Weak transcription HUVEC blood vessel
3 chr2:67602200-67617000 Weak transcription Aorta Aorta
4 chr2:67602600-67615800 Weak transcription NHLF lung
5 chr2:67606600-67624200 Weak transcription Pancreas Pancrea
6 chr2:67611000-67615800 Weak transcription NH-A brain
7 chr2:67612000-67616000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr2:67613200-67621600 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chr2:67613800-67616200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:67615200-67618000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:67615600-67615800 Enhancers HUES48 Cell Line embryonic stem cell
12 chr2:67615600-67617800 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr2:67615600-67617800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr2:67615600-67617800 Enhancers Muscle Satellite Cultured Cells --
15 chr2:67615600-67618800 Enhancers ES-I3 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links