Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:41120371-41120436 | Rare:7 | ||||
chr4:52712220-52712527 | Common:4; Rare:80 | ||||
chr4:52722378-52722561 | Common:1; Rare:46 | ||||
chr4:52945569-52945733 | Rare:25 | ||||
chr4:53485147-53485595 | Common:4; Rare:70 | ||||
chr4:53592832-53592957 | Common:2; Rare:25 | ||||
chr4:54267286-54267716 | Common:3; Rare:110; Clinvar:30; Clinvar (benign):18 | ||||
chr4:55397797-55397929 | Common:2; Rare:33 | ||||
chr4:55890086-55890326 | Rare:54 | ||||
chr4:55947908-55948154 | Common:2; Rare:42 | ||||
chr4:57032426-57032646 | Common:1; Rare:58 | ||||
chr4:75725177-75725250 | Rare:23 | ||||
chr4:77820248-77820377 | Rare:52 | ||||
chr4:81470485-81470692 | Common:1; Rare:42 | ||||
chr4:82496102-82496450 | Rare:73 |