Variant report

Variant rs576215690
Chromosome Location chr11:58539685-58539686
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58537600-58539800 Enhancers NHEK skin
2 chr11:58537600-58540200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:58537600-58540200 Flanking Active TSS K562 blood
4 chr11:58539000-58541000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr11:58539000-58542600 Enhancers Fetal Intestine Small intestine
6 chr11:58539200-58541200 Weak transcription Adipose Nuclei Adipose
7 chr11:58539400-58540000 Enhancers HepG2 liver
8 chr11:58539600-58543000 Enhancers Fetal Intestine Large intestine

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