Variant report

Variant rs13051498
Chromosome Location chr21:47453597-47453598
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47445600-47458600 Weak transcription Stomach Mucosa stomach
2 chr21:47448400-47455400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr21:47449400-47455400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr21:47449400-47458400 Weak transcription Right Atrium heart
5 chr21:47449600-47453800 Weak transcription Rectal Smooth Muscle rectum
6 chr21:47449600-47455600 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr21:47451800-47455600 Weak transcription Left Ventricle heart
8 chr21:47451800-47458000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:47452400-47454000 Enhancers Placenta Placenta
10 chr21:47452600-47454200 Enhancers Fetal Stomach stomach
11 chr21:47453200-47453800 Enhancers Stomach Smooth Muscle stomach
12 chr21:47453200-47454000 ZNF genes & repeats Fetal Intestine Large intestine
13 chr21:47453200-47454400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr21:47453400-47454000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
15 chr21:47453400-47454200 Enhancers Fetal Lung lung
16 chr21:47453400-47454200 Flanking Active TSS Ovary ovary

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