Variant report

Variant rs1298056
Chromosome Location chr10:92494971-92494972
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:92492400-92495000 Enhancers iPS-15b Cell Line embryonic stem cell
2 chr10:92492600-92495400 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr10:92492800-92501200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr10:92492800-92503000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr10:92494000-92495000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr10:92494400-92495000 Enhancers H1 Cell Line embryonic stem cell
7 chr10:92494400-92495000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
8 chr10:92494400-92495000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr10:92494600-92495400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr10:92494600-92500000 Weak transcription NHEK skin
11 chr10:92494600-92501600 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr10:92494600-92510800 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr10:92494800-92495000 ZNF genes & repeats Aorta Aorta
14 chr10:92494800-92501800 Weak transcription iPS-20b Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links