Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:81683721-81684052 | Common:4; Rare:165 | ||||
chr17:81703297-81703467 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr17:82450726-82450911 | Common:2; Rare:71 | ||||
chr17:82458518-82458711 | Common:2; Rare:59 | ||||
chr18:812225-812406 | Common:1; Rare:69 | ||||
chr18:2571497-2571583 | Rare:25 | ||||
chr18:3261815-3262217 | Common:6; Rare:129 | ||||
chr18:9102519-9102764 | Common:1; Rare:100; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9914203-9914256 | Rare:31 | ||||
chr18:11851077-11851427 | Common:2; Rare:107 | ||||
chr18:11908276-11908421 | Rare:42 | ||||
chr18:12702671-12703084 | Common:3; Rare:166 | ||||
chr18:13726462-13726714 | Common:3; Rare:100 | ||||
chr18:21600666-21600852 | Rare:42 | ||||
chr18:21612179-21612418 | Common:1; Rare:73 |