Variant report

Variant rs72649953
Chromosome Location chr1:210297082-210297083
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210283000-210298000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:210291800-210297200 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr1:210291800-210297400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr1:210295600-210298600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr1:210295800-210298000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr1:210296200-210299800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:210296400-210297200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:210296600-210297200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr1:210296600-210298000 Enhancers HMEC breast
10 chr1:210296600-210298400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:210296600-210298800 Enhancers NH-A brain
12 chr1:210296600-210299400 Enhancers NHDF-Ad bronchial
13 chr1:210296800-210297200 Enhancers NHLF lung
14 chr1:210296800-210298000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr1:210296800-210298200 Enhancers NHEK skin
16 chr1:210297000-210297400 Enhancers Pancreatic Islets Pancreatic Islet
17 chr1:210297000-210297600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links