Variant report
Variant | rs138939147 |
---|---|
Chromosome Location | chr21:16521970-16521971 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:16514600-16529600 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr21:16517200-16526800 | Weak transcription | Pancreas | Pancrea |
3 | chr21:16520800-16522000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr21:16521400-16522000 | Enhancers | Fetal Intestine Small | intestine |
5 | chr21:16521400-16522200 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
6 | chr21:16521400-16522200 | Enhancers | Fetal Intestine Large | intestine |
7 | chr21:16521400-16529600 | Weak transcription | Adipose Nuclei | Adipose |
8 | chr21:16521600-16522000 | Enhancers | Sigmoid Colon | Sigmoid Colon |
9 | chr21:16521600-16525600 | Enhancers | HepG2 | liver |
10 | chr21:16521800-16524800 | Enhancers | Liver | Liver |