Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:47530919-47531226 | Common:2; Rare:83 | ||||
chr17:47649420-47649444 | Rare:4 | ||||
chr17:47649518-47649969 | Common:1; Rare:165 | ||||
chr17:47650134-47650443 | Rare:109 | ||||
chr17:47693774-47694096 | Common:1; Rare:53 | ||||
chr17:47695054-47695075 | Rare:3 | ||||
chr17:47821744-47821899 | Common:1; Rare:34 | ||||
chr17:47831491-47831656 | Rare:49 | ||||
chr17:47841118-47841408 | Rare:62 | ||||
chr17:47896494-47896565 | Rare:18 | ||||
chr17:47941348-47941802 | Rare:118; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr17:47957664-47958026 | Common:2; Rare:60 | ||||
chr17:47970740-47971176 | Common:4; Rare:104 | ||||
chr17:48048039-48048409 | Common:1; Rare:102 | ||||
chr17:48048599-48048813 | Common:4; Rare:31 |