Variant report

Variant rs35966851
Chromosome Location chr21:47483051-47483052
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47479400-47485200 Enhancers NHDF-Ad bronchial
2 chr21:47480600-47485000 Weak transcription Right Atrium heart
3 chr21:47480800-47483800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr21:47481200-47484800 Weak transcription Ovary ovary
5 chr21:47481200-47485000 Weak transcription Colon Smooth Muscle Colon
6 chr21:47481400-47483400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:47481400-47483600 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
8 chr21:47481600-47483600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
9 chr21:47482200-47485200 Weak transcription Placenta Amnion Placenta Amnion
10 chr21:47482400-47483400 ZNF genes & repeats NHLF lung
11 chr21:47482600-47483200 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
12 chr21:47482600-47483600 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr21:47482800-47483200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr21:47482800-47483600 ZNF genes & repeats Adipose Nuclei Adipose
15 chr21:47483000-47484800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr21:47483000-47484800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr21:47483000-47485000 Weak transcription Osteobl bone
18 chr21:47483000-47488400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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