Variant report

Variant rs391465
Chromosome Location chr22:22747677-22747678
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:2 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22743200-22748800 Weak transcription Fetal Intestine Large intestine
2 chr22:22747600-22747800 ZNF genes & repeats Primary B cells from cord blood blood

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