Variant report

Variant rs346683
Chromosome Location chr1:120138931-120138932
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:120115200-120160800 Weak transcription Gastric stomach
2 chr1:120130200-120139000 Weak transcription Left Ventricle heart
3 chr1:120133600-120144800 Weak transcription Placenta Placenta
4 chr1:120135200-120151000 Weak transcription Fetal Stomach stomach
5 chr1:120136400-120139200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:120136400-120139600 Enhancers HMEC breast
7 chr1:120136800-120139200 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr1:120136800-120142800 Weak transcription Fetal Intestine Small intestine
9 chr1:120137200-120139400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:120137600-120139000 Enhancers NHEK skin
11 chr1:120138200-120139400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:120138400-120139000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
13 chr1:120138400-120139000 Enhancers HUVEC blood vessel
14 chr1:120138400-120140600 Weak transcription Brain Angular Gyrus brain
15 chr1:120138800-120139000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr1:120138800-120139200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links