Variant report

Variant rs11935382
Chromosome Location chr4:127770795-127770796
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:127765200-127771600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr4:127770200-127772200 Enhancers Osteobl bone
3 chr4:127770200-127772800 Enhancers NHEK skin
4 chr4:127770200-127773000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr4:127770200-127773200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:127770200-127773400 Enhancers NH-A brain
7 chr4:127770200-127773400 Enhancers NHDF-Ad bronchial
8 chr4:127770400-127772800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:127770600-127771000 ZNF genes & repeats K562 blood
10 chr4:127770600-127771800 Enhancers NHLF lung
11 chr4:127770600-127772600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr4:127770600-127773400 Enhancers HMEC breast

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