| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:10116734-10117089 | Common:6; Rare:172 | ||||
| chr4:10457330-10457448 | Common:4; Rare:49 | ||||
| chr4:15339836-15339988 | Rare:36 | ||||
| chr4:15479012-15479251 | Common:2; Rare:50 | ||||
| chr4:15655295-15655481 | Common:1; Rare:85 | ||||
| chr4:15681514-15681869 | Common:3; Rare:121 | ||||
| chr4:17577327-17577544 | Rare:103 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 | ||||
| chr4:17810681-17811073 | Common:4; Rare:123 | ||||
| chr4:23890030-23890133 | Rare:16 | ||||
| chr4:24584389-24584725 | Common:1; Rare:104 | ||||
| chr4:25160411-25160704 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914318 | Common:2; Rare:114 | ||||
| chr4:26320898-26321046 | Rare:53; Clinvar (benign):1 | ||||
| chr4:26860563-26860791 | Common:1; Rare:70 |