| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1201541-1201790 | Rare:68 | ||||
| chr4:1720546-1720659 | Rare:38 | ||||
| chr4:2468871-2469167 | Common:4; Rare:108 | ||||
| chr4:2812043-2812308 | Rare:42 | ||||
| chr4:2843699-2844022 | Common:3; Rare:117 | ||||
| chr4:2934777-2934931 | Common:4; Rare:72 | ||||
| chr4:2963332-2963639 | Common:3; Rare:112 | ||||
| chr4:3074576-3074692 | Common:2; Rare:36 | ||||
| chr4:3532208-3532311 | Rare:32; Clinvar (pathogenic):2 | ||||
| chr4:4248198-4248276 | Common:1; Rare:32 | ||||
| chr4:4290091-4290287 | Common:5; Rare:81 | ||||
| chr4:4541929-4542321 | Common:2; Rare:140 | ||||
| chr4:5019430-5019544 | Common:1; Rare:40 | ||||
| chr4:6640543-6641103 | Common:4; Rare:191 | ||||
| chr4:6909391-6909478 | Rare:22 |