| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1171134-1171297 | Rare:67 | ||||
| chr4:1171404-1171605 | Rare:65 | ||||
| chr4:1346933-1347213 | Common:4; Rare:78 | ||||
| chr4:1347876-1348109 | Common:1; Rare:73 | ||||
| chr4:1720494-1720651 | Rare:48 | ||||
| chr4:1856097-1856413 | Rare:81 | ||||
| chr4:1975137-1975338 | Rare:56 | ||||
| chr4:1991982-1992097 | Common:1; Rare:28 | ||||
| chr4:2041927-2042022 | Rare:40 | ||||
| chr4:2468871-2469197 | Common:5; Rare:130 | ||||
| chr4:2843679-2844000 | Common:3; Rare:120 | ||||
| chr4:2934777-2934928 | Common:4; Rare:71 | ||||
| chr4:2963346-2963639 | Common:3; Rare:103 | ||||
| chr4:3074605-3074700 | Common:2; Rare:36 | ||||
| chr4:3532208-3532343 | Rare:50; Clinvar (pathogenic):2 |