Variant report

Variant rs1492906
Chromosome Location chr1:172712707-172712708
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172711400-172714000 Weak transcription Primary T cells from cord blood blood
2 chr1:172712000-172712800 Enhancers Muscle Satellite Cultured Cells --
3 chr1:172712000-172712800 Enhancers NHLF lung
4 chr1:172712000-172714000 Weak transcription Primary T helper naive cells from peripheral blood blood
5 chr1:172712000-172714000 Weak transcription Primary T helper cells PMA-I stimulated --
6 chr1:172712000-172716400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:172712000-172716400 Enhancers HMEC breast
8 chr1:172712000-172717000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:172712200-172712800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr1:172712200-172712800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:172712200-172716400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:172712400-172714000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:172712400-172714400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:172712600-172714000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
15 chr1:172712600-172714000 Weak transcription HUVEC blood vessel

Quick Search:


  
Input of quick search could be:

what's new

Quick links