Variant report

Variant rs11900055
Chromosome Location chr2:234731301-234731302
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234713200-234731400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:234727000-234731400 Weak transcription A549 lung
3 chr2:234730000-234732200 Enhancers Duodenum Mucosa Duodenum
4 chr2:234730800-234732000 Flanking Active TSS Liver Liver
5 chr2:234731000-234731800 Enhancers Fetal Intestine Small intestine
6 chr2:234731200-234731400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin

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