Variant report

Variant rs4277072
Chromosome Location chr11:26248041-26248042
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26241600-26249200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr11:26241600-26249800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr11:26246200-26248400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr11:26247400-26248600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr11:26247600-26248400 Weak transcription NHDF-Ad bronchial
6 chr11:26247800-26248600 Weak transcription Fetal Brain Male brain
7 chr11:26248000-26250200 Enhancers HUVEC blood vessel
8 chr11:26248000-26251800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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