Variant report

Variant rs566185006
Chromosome Location chr14:66284900-66284901
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:66276200-66288000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:66281600-66293400 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr14:66284200-66285200 Genic enhancers Pancreas Pancrea
4 chr14:66284200-66285600 ZNF genes & repeats Fetal Kidney kidney
5 chr14:66284200-66285600 Enhancers Gastric stomach
6 chr14:66284600-66285600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr14:66284600-66285800 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr14:66284600-66286000 ZNF genes & repeats H9 Cell Line embryonic stem cell
9 chr14:66284800-66285000 Strong transcription Spleen Spleen
10 chr14:66284800-66285600 Flanking Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr14:66284800-66285800 Active TSS Fetal Lung lung

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