| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74098987-74099131 | Common:1; Rare:54 | ||||
| chr4:74099176-74099461 | Common:3; Rare:65 | ||||
| chr4:74157818-74158216 | Common:2; Rare:174 | ||||
| chr4:74308320-74308661 | Common:1; Rare:78 | ||||
| chr4:75514260-75514505 | Common:1; Rare:86 | ||||
| chr4:75514664-75514770 | Rare:27 | ||||
| chr4:75630521-75630684 | Rare:39 | ||||
| chr4:75673063-75673692 | Common:1; Rare:222 | ||||
| chr4:75724367-75724885 | Common:2; Rare:166 | ||||
| chr4:75940268-75940354 | Common:1; Rare:22 | ||||
| chr4:75990888-75990970 | Rare:34 | ||||
| chr4:76148318-76148594 | Common:5; Rare:81 | ||||
| chr4:76213538-76214020 | Common:4; Rare:169; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:76306367-76306441 | Common:1; Rare:13 | ||||
| chr4:76949559-76949883 | Common:2; Rare:107 |