Variant report

Variant rs138939147
Chromosome Location chr21:16521970-16521971
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
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

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