| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:673814-673957 | Common:1; Rare:55 | ||||
| chr4:674246-674566 | Common:2; Rare:151 | ||||
| chr4:2468878-2469159 | Common:3; Rare:101 | ||||
| chr4:4248187-4248261 | Common:2; Rare:34 | ||||
| chr4:4290117-4290235 | Common:1; Rare:44 | ||||
| chr4:15681478-15681875 | Common:4; Rare:138 | ||||
| chr4:17810731-17810996 | Common:2; Rare:70 | ||||
| chr4:39458853-39459075 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr4:39638829-39639140 | Common:1; Rare:115 | ||||
| chr4:41990407-41990563 | Common:1; Rare:58 | ||||
| chr4:56467542-56467632 | Rare:37 | ||||
| chr4:67701124-67701341 | Common:4; Rare:103 | ||||
| chr4:75514273-75514470 | Common:1; Rare:67 | ||||
| chr4:75673351-75673665 | Common:1; Rare:126 | ||||
| chr4:75724412-75724713 | Common:1; Rare:87 |