Variant report

Variant rs7855470
Chromosome Location chr9:93839462-93839463
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93834400-93839800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr9:93834800-93839800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:93836000-93839800 Weak transcription Fetal Intestine Large intestine
4 chr9:93836600-93840000 Weak transcription Lung lung
5 chr9:93836600-93841200 Enhancers Placenta Placenta
6 chr9:93837800-93839800 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr9:93837800-93840000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr9:93838000-93840000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr9:93838200-93840400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr9:93838400-93839800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:93839000-93839600 ZNF genes & repeats Fetal Intestine Small intestine
12 chr9:93839000-93840200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:93839400-93840400 Enhancers Placenta Amnion Placenta Amnion

Quick Search:


  
Input of quick search could be:

what's new

Quick links