| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:3074369-3074715 | Common:7; Rare:106 | ||||
| chr4:3484771-3484792 | Common:1; Rare:3 | ||||
| chr4:3485403-3485518 | Common:4; Rare:33; Clinvar (benign):2 | ||||
| chr4:4248198-4248318 | Common:2; Rare:42 | ||||
| chr4:4290048-4290332 | Common:5; Rare:105 | ||||
| chr4:4541978-4542212 | Common:2; Rare:91 | ||||
| chr4:6640541-6640720 | Common:2; Rare:74 | ||||
| chr4:6709794-6709980 | Common:1; Rare:56 | ||||
| chr4:6986994-6987307 | Common:2; Rare:102 | ||||
| chr4:7043961-7044015 | Rare:8 | ||||
| chr4:10116709-10117113 | Common:9; Rare:201 | ||||
| chr4:11428881-11429063 | Common:1; Rare:55 | ||||
| chr4:13484301-13484458 | Rare:59 | ||||
| chr4:15002895-15002951 | Rare:26 | ||||
| chr4:15681632-15681752 | Common:3; Rare:45 |