Variant report

Variant rs10099662
Chromosome Location chr8:1326444-1326445
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:1315800-1336800 Weak transcription Right Atrium heart
2 chr8:1324800-1326600 Weak transcription Fetal Brain Male brain
3 chr8:1325400-1329600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:1326200-1326600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr8:1326200-1326800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr8:1326200-1326800 Active TSS H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr8:1326400-1326600 ZNF genes & repeats Pancreas Pancrea
8 chr8:1326400-1326800 ZNF genes & repeats H9 Cell Line embryonic stem cell
9 chr8:1326400-1326800 Enhancers Fetal Brain Female brain
10 chr8:1326400-1326800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
11 chr8:1326400-1326800 ZNF genes & repeats Spleen Spleen

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