Variant report

Variant rs374192
Chromosome Location chr20:14967506-14967507
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14964600-14971600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr20:14964800-14967800 Enhancers HUVEC blood vessel
3 chr20:14965000-14968000 Enhancers Liver Liver
4 chr20:14965400-14967600 Enhancers Pancreas Pancrea
5 chr20:14965400-14968000 Enhancers Fetal Kidney kidney
6 chr20:14965400-14968000 Enhancers Hela-S3 cervix
7 chr20:14967200-14967600 Flanking Active TSS Fetal Intestine Small intestine
8 chr20:14967200-14967600 Flanking Active TSS A549 lung
9 chr20:14967200-14967600 Flanking Active TSS HepG2 liver
10 chr20:14967400-14967600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr20:14967400-14967600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr20:14967400-14967600 Flanking Active TSS Duodenum Mucosa Duodenum
13 chr20:14967400-14967600 Enhancers Pancreatic Islets Pancreatic Islet
14 chr20:14967400-14967600 Flanking Active TSS Rectal Mucosa Donor 29 rectum
15 chr20:14967400-14967600 Flanking Active TSS Rectal Mucosa Donor 31 rectum
16 chr20:14967400-14967600 Enhancers Stomach Mucosa stomach
17 chr20:14967400-14968000 Enhancers Fetal Intestine Large intestine
18 chr20:14967400-14971600 Weak transcription HMEC breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links