Variant report

Variant rs1868947
Chromosome Location chr19:52101918-52101919
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52098400-52102000 Weak transcription Right Atrium heart
2 chr19:52098600-52105000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr19:52098600-52110400 Weak transcription Brain Cingulate Gyrus brain
4 chr19:52098800-52110600 Weak transcription Brain Anterior Caudate brain
5 chr19:52099400-52110800 Weak transcription Pancreas Pancrea
6 chr19:52101400-52102000 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
7 chr19:52101600-52102200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
8 chr19:52101800-52102000 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
9 chr19:52101800-52102000 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr19:52101800-52102000 Enhancers Placenta Placenta
11 chr19:52101800-52102000 Flanking Active TSS Gastric stomach
12 chr19:52101800-52102400 ZNF genes & repeats Spleen Spleen

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