Variant report

Variant rs7547709
Chromosome Location chr1:210161291-210161292
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210159400-210162000 Weak transcription NHEK skin
2 chr1:210159400-210163000 Weak transcription H1 Cell Line embryonic stem cell
3 chr1:210159400-210166600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr1:210159600-210166200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:210159600-210168200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:210160800-210161600 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr1:210161000-210161800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:210161200-210161600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr1:210161200-210162000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links