Variant report

Variant rs73933824
Chromosome Location chr2:51519311-51519312
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51517000-51520200 Weak transcription Liver Liver
2 chr2:51518000-51521200 Enhancers iPS-15b Cell Line embryonic stem cell
3 chr2:51518800-51519400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr2:51518800-51519600 Flanking Active TSS HUES48 Cell Line embryonic stem cell
5 chr2:51518800-51519600 Flanking Active TSS HUES64 Cell Line embryonic stem cell
6 chr2:51519000-51519600 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
7 chr2:51519000-51519800 Enhancers Cortex derived primary cultured neurospheres brain
8 chr2:51519200-51519400 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr2:51519200-51519600 Flanking Active TSS HUES6 Cell Line embryonic stem cell
10 chr2:51519200-51519600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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