| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197850988-197851009 | Rare:1 | ||||
| chr4:1802616-1802944 | Common:1; Rare:115 | ||||
| chr4:1806050-1806326 | Common:2; Rare:100; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr4:7433431-7433504 | Common:1; Rare:31 | ||||
| chr4:7433648-7433716 | Common:2; Rare:29 | ||||
| chr4:7434266-7434355 | Common:2; Rare:36 | ||||
| chr4:24966180-24966464 | Common:2; Rare:38 | ||||
| chr4:38664868-38665122 | Common:1; Rare:65 | ||||
| chr4:56976899-56976992 | Common:1; Rare:32 | ||||
| chr4:77820248-77820382 | Rare:53 | ||||
| chr4:118265828-118265911 | Common:2; Rare:23 | ||||
| chr4:118279109-118279190 | Common:3; Rare:20 | ||||
| chr4:119454600-119454861 | Common:12; Rare:87 | ||||
| chr4:151100791-151101161 | Rare:76 | ||||
| chr5:8457606-8457739 | Common:1; Rare:38 |