Variant report

Variant rs7000889
Chromosome Location chr8:42547582-42547583
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:42544000-42561200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr8:42545200-42547800 Weak transcription HSMM muscle
3 chr8:42546400-42547600 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr8:42546800-42547800 Weak transcription HepG2 liver
5 chr8:42547200-42547800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr8:42547200-42548000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr8:42547400-42548000 Enhancers Adipose Nuclei Adipose
8 chr8:42547400-42548000 Enhancers Dnd41 blood
9 chr8:42547400-42548200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr8:42547400-42548400 Enhancers Primary T killer memory cells from peripheral blood blood
11 chr8:42547400-42548400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:42547400-42548600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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