| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7042930-7043900 | Common:7; Rare:439 | ||||
| chr4:7068002-7068421 | Common:18; Rare:281 | ||||
| chr4:8158800-8159090 | Common:4; Rare:191 | ||||
| chr4:8428368-8428548 | Common:5; Rare:121 | ||||
| chr4:8440680-8440838 | Rare:114 | ||||
| chr4:10021373-10021557 | Rare:69 | ||||
| chr4:10116687-10117104 | Common:16; Rare:388 | ||||
| chr4:13627579-13627901 | Common:2; Rare:172 | ||||
| chr4:15002308-15002489 | Common:1; Rare:59 | ||||
| chr4:15002580-15002990 | Common:5; Rare:278 | ||||
| chr4:15655292-15655530 | Common:2; Rare:197 | ||||
| chr4:15681389-15681880 | Common:7; Rare:312 | ||||
| chr4:16226400-16226695 | Common:6; Rare:195 | ||||
| chr4:17512036-17512314 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17576864-17577216 | Common:10; Rare:201 |