| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2963328-2963605 | Common:2; Rare:97 | ||||
| chr4:3074516-3074692 | Common:4; Rare:54 | ||||
| chr4:3292754-3293060 | Common:2; Rare:119 | ||||
| chr4:3532216-3532258 | Rare:14; Clinvar (pathogenic):1 | ||||
| chr4:4248187-4248266 | Common:2; Rare:37 | ||||
| chr4:4290117-4290277 | Common:3; Rare:64 | ||||
| chr4:4541960-4542212 | Common:2; Rare:102 | ||||
| chr4:5019422-5019524 | Common:1; Rare:40 | ||||
| chr4:5708957-5709048 | Rare:24 | ||||
| chr4:6640537-6640720 | Common:2; Rare:77 | ||||
| chr4:6709815-6710004 | Common:2; Rare:56 | ||||
| chr4:6909391-6909473 | Rare:21 | ||||
| chr4:6987014-6987257 | Common:2; Rare:73 | ||||
| chr4:7068028-7068373 | Common:5; Rare:118 | ||||
| chr4:7939797-7940110 | Common:3; Rare:125 |