Variant report

Variant rs371026645
Chromosome Location chr11:58539485-58539486
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58537600-58539600 Flanking Active TSS Fetal Intestine Large intestine
2 chr11:58537600-58539600 Enhancers HMEC breast
3 chr11:58537600-58539800 Enhancers NHEK skin
4 chr11:58537600-58540200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr11:58537600-58540200 Flanking Active TSS K562 blood
6 chr11:58539000-58541000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:58539000-58542600 Enhancers Fetal Intestine Small intestine
8 chr11:58539200-58541200 Weak transcription Adipose Nuclei Adipose
9 chr11:58539400-58540000 Enhancers HepG2 liver

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