Variant report

Variant rs398439
Chromosome Location chr20:14966995-14966996
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr20:14965200-14967200 Enhancers Fetal Intestine Small intestine
5 chr20:14965400-14967400 Enhancers Rectal Mucosa Donor 31 rectum
6 chr20:14965400-14967600 Enhancers Pancreas Pancrea
7 chr20:14965400-14968000 Enhancers Fetal Kidney kidney
8 chr20:14965400-14968000 Enhancers Hela-S3 cervix
9 chr20:14965800-14967200 Enhancers Pancreatic Islets Pancreatic Islet
10 chr20:14966000-14967200 Weak transcription Duodenum Mucosa Duodenum
11 chr20:14966000-14967400 Enhancers HMEC breast
12 chr20:14966200-14967400 Weak transcription Stomach Mucosa stomach
13 chr20:14966400-14967000 Weak transcription Rectal Mucosa Donor 29 rectum
14 chr20:14966600-14967000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr20:14966600-14967000 Enhancers Aorta Aorta
16 chr20:14966600-14967400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr20:14966800-14967200 Active TSS A549 lung
18 chr20:14966800-14967200 Enhancers HepG2 liver
19 chr20:14966800-14967400 Weak transcription Fetal Intestine Large intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links