Variant report

Variant rs144273568
Chromosome Location chr7:41098348-41098349
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41088400-41099000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:41092200-41098800 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr7:41095000-41100200 Weak transcription Muscle Satellite Cultured Cells --
4 chr7:41095200-41100000 Weak transcription Aorta Aorta
5 chr7:41095600-41100600 Weak transcription HSMM muscle
6 chr7:41097800-41098600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr7:41097800-41098800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:41098000-41098600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr7:41098000-41099000 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
10 chr7:41098000-41099800 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
11 chr7:41098200-41098400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:41098200-41098800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
13 chr7:41098200-41099800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr7:41098200-41100000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
15 chr7:41098200-41100200 Bivalent Enhancer H1 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links