Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:48269773-48269971 | Common:2; Rare:50 | ||||
chr4:52659238-52659444 | Common:1; Rare:69 | ||||
chr4:53377801-53377899 | Rare:33 | ||||
chr4:56387423-56387534 | Rare:38 | ||||
chr4:56435473-56435759 | Common:5; Rare:104 | ||||
chr4:56467552-56467699 | Common:2; Rare:61; Clinvar (benign):5 | ||||
chr4:56656412-56656615 | Common:3; Rare:33 | ||||
chr4:56977537-56977765 | Common:2; Rare:87 | ||||
chr4:67701117-67701362 | Common:4; Rare:114 | ||||
chr4:68349966-68350236 | Common:2; Rare:97 | ||||
chr4:70688200-70688587 | Common:2; Rare:97 | ||||
chr4:70688929-70689063 | Rare:52 | ||||
chr4:70902168-70902378 | Common:5; Rare:78 | ||||
chr4:70993498-70993717 | Common:4; Rare:67 | ||||
chr4:73258469-73258609 | Common:1; Rare:46 |