Variant report

Variant rs10947519
Chromosome Location chr6:11688889-11688890
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11685000-11689400 Enhancers Fetal Intestine Large intestine
2 chr6:11685200-11693000 Weak transcription Spleen Spleen
3 chr6:11686600-11689000 Weak transcription HSMM muscle
4 chr6:11686600-11701400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:11686600-11702400 Weak transcription HSMMtube muscle
6 chr6:11687200-11689200 Enhancers Fetal Heart heart
7 chr6:11687200-11689200 Enhancers Fetal Stomach stomach
8 chr6:11687200-11689400 Enhancers Brain Germinal Matrix brain
9 chr6:11687400-11689000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr6:11688400-11689000 Enhancers HUES48 Cell Line embryonic stem cell
11 chr6:11688600-11689000 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr6:11688600-11689200 Enhancers Fetal Kidney kidney
13 chr6:11688600-11689200 Enhancers Fetal Lung lung
14 chr6:11688600-11689400 Enhancers Fetal Intestine Small intestine
15 chr6:11688600-11689400 Enhancers Ovary ovary
16 chr6:11688800-11692600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr6:11688800-11711000 Weak transcription ES-I3 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links