Variant report

Variant rs11250658
Chromosome Location chr10:1643672-1643673
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1634600-1648200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:1637600-1643800 Weak transcription Fetal Brain Male brain
3 chr10:1642400-1644000 Enhancers Dnd41 blood
4 chr10:1643000-1645000 Bivalent Enhancer Fetal Lung lung
5 chr10:1643200-1643800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr10:1643200-1644000 Flanking Active TSS NHEK skin
7 chr10:1643200-1644200 Enhancers Fetal Stomach stomach
8 chr10:1643200-1645200 Weak transcription Esophagus oesophagus
9 chr10:1643400-1643800 Enhancers GM12878-XiMat blood
10 chr10:1643400-1643800 Enhancers HMEC breast
11 chr10:1643400-1644000 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr10:1643400-1644600 Enhancers Fetal Thymus thymus
13 chr10:1643600-1643800 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
14 chr10:1643600-1644000 Enhancers Fetal Brain Female brain
15 chr10:1643600-1644200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links