Variant report

Variant rs181385492
Chromosome Location chr1:120106618-120106619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:120092800-120116600 Weak transcription Spleen Spleen
2 chr1:120097200-120107400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:120097600-120107400 Weak transcription Brain Hippocampus Middle brain
4 chr1:120105000-120108000 Enhancers Fetal Lung lung
5 chr1:120105000-120108800 Enhancers Fetal Intestine Large intestine
6 chr1:120105200-120108600 Enhancers Fetal Intestine Small intestine
7 chr1:120105400-120106800 Enhancers Ovary ovary
8 chr1:120105800-120106800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr1:120105800-120106800 Weak transcription Placenta Placenta
10 chr1:120106200-120106800 Enhancers Fetal Stomach stomach
11 chr1:120106200-120107200 Enhancers Monocytes-CD14+_RO01746 blood
12 chr1:120106200-120107400 Enhancers Primary monocytes fromperipheralblood blood
13 chr1:120106600-120106800 Enhancers Lung lung
14 chr1:120106600-120106800 Enhancers Right Atrium heart
15 chr1:120106600-120107400 Enhancers GM12878-XiMat blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links