Variant report

Variant rs4880532
Chromosome Location chr10:1728711-1728712
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1718400-1734200 Weak transcription GM12878-XiMat blood
2 chr10:1720600-1729800 Weak transcription Fetal Brain Female brain
3 chr10:1727400-1729600 Enhancers Fetal Intestine Large intestine
4 chr10:1727400-1729600 Enhancers Fetal Intestine Small intestine
5 chr10:1728000-1728800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr10:1728000-1728800 Enhancers Spleen Spleen
7 chr10:1728000-1729400 Enhancers Duodenum Mucosa Duodenum
8 chr10:1728200-1738000 Weak transcription Pancreas Pancrea
9 chr10:1728400-1731200 Enhancers Fetal Brain Male brain

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