Variant report

Variant rs9621625
Chromosome Location chr22:33451858-33451859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33448600-33452800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr22:33449400-33452000 Flanking Active TSS HUES48 Cell Line embryonic stem cell
3 chr22:33449400-33453600 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
4 chr22:33450000-33452400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr22:33450000-33452400 Enhancers HepG2 liver
6 chr22:33450600-33452000 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
7 chr22:33450800-33452800 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
8 chr22:33450800-33454600 Active TSS ES-WA7 Cell Line embryonic stem cell
9 chr22:33451200-33452000 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
10 chr22:33451200-33453000 Active TSS Fetal Brain Female brain
11 chr22:33451200-33454800 Bivalent/Poised TSS Brain Angular Gyrus brain
12 chr22:33451400-33452000 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
13 chr22:33451600-33452000 Flanking Active TSS ES-UCSF4 Cell Line embryonic stem cell
14 chr22:33451800-33452000 Flanking Bivalent TSS/Enh ES-I3 Cell Line embryonic stem cell
15 chr22:33451800-33452200 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
16 chr22:33451800-33452600 Active TSS Brain Anterior Caudate brain

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