Variant report

Variant rs6689291
Chromosome Location chr1:172426858-172426859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172422600-172435400 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:172423200-172429000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:172423200-172429200 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr1:172423400-172434600 Weak transcription HSMMtube muscle
5 chr1:172423600-172432000 Weak transcription Primary neutrophils fromperipheralblood blood
6 chr1:172425800-172435400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr1:172426000-172436000 Weak transcription Fetal Intestine Large intestine
8 chr1:172426400-172427200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:172426400-172427200 Enhancers K562 blood
10 chr1:172426400-172428200 Weak transcription Fetal Muscle Trunk muscle
11 chr1:172426400-172434600 Weak transcription Fetal Muscle Leg muscle
12 chr1:172426600-172427000 Enhancers Adipose Nuclei Adipose
13 chr1:172426600-172427000 Enhancers HepG2 liver
14 chr1:172426800-172427200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links