Variant report

Variant rs332796
Chromosome Location chr1:174696280-174696281
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174678200-174708600 Weak transcription Primary T cells from cord blood blood
2 chr1:174678600-174706400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr1:174682200-174704800 Weak transcription Primary B cells from peripheral blood blood
4 chr1:174687800-174705200 Weak transcription Primary B cells from cord blood blood
5 chr1:174695400-174696600 Enhancers GM12878-XiMat blood
6 chr1:174695800-174696400 Enhancers Fetal Intestine Small intestine
7 chr1:174696000-174696400 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr1:174696000-174696600 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:174696000-174696800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:174696000-174696800 Enhancers Fetal Intestine Large intestine
11 chr1:174696200-174696400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:174696200-174696600 Enhancers H1 Cell Line embryonic stem cell
13 chr1:174696200-174696600 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr1:174696200-174701800 Weak transcription Liver Liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links