Variant report

Variant rs114179278
Chromosome Location chr12:31357625-31357626
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31355200-31362600 Enhancers HMEC breast
2 chr12:31356400-31358000 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr12:31356400-31360800 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr12:31356600-31358200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr12:31356600-31360400 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr12:31356800-31357800 Weak transcription NHEK skin
7 chr12:31357000-31358200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr12:31357000-31360400 Enhancers HUES64 Cell Line embryonic stem cell
9 chr12:31357000-31360600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr12:31357200-31359000 Weak transcription H1 Cell Line embryonic stem cell
11 chr12:31357200-31359000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr12:31357600-31358400 Enhancers Primary B cells from peripheral blood blood
13 chr12:31357600-31358400 Enhancers Primary T cells from cord blood blood
14 chr12:31357600-31358400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr12:31357600-31358600 Enhancers Primary B cells from cord blood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links