| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7068002-7068392 | Common:8; Rare:138 | ||||
| chr4:8440692-8440769 | Rare:26 | ||||
| chr4:10116655-10117092 | Common:8; Rare:203 | ||||
| chr4:13627669-13627853 | Common:1; Rare:57 | ||||
| chr4:15681466-15681863 | Common:3; Rare:138 | ||||
| chr4:16898379-16898506 | Rare:36 | ||||
| chr4:17614581-17614672 | Common:1; Rare:49 | ||||
| chr4:17810706-17811006 | Common:2; Rare:88 | ||||
| chr4:24584325-24584383 | Rare:20 | ||||
| chr4:25160392-25160736 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233845-25234094 | Rare:103 | ||||
| chr4:25914051-25914288 | Common:2; Rare:101 | ||||
| chr4:38867666-38867826 | Common:1; Rare:64 | ||||
| chr4:39366321-39366431 | Rare:35 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 |