Variant report

Variant rs552672608
Chromosome Location chr6:26705917-26705918
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:2 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26702000-26706400 Weak transcription H9 Cell Line embryonic stem cell
2 chr6:26705600-26706000 Flanking Bivalent TSS/Enh HepG2 liver

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