| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929931-98930445 | Common:2; Rare:112 | ||||
| chr4:98995164-98995345 | Common:5; Rare:38 | ||||
| chr4:98995264-98996183 | Common:42; Rare:1034 | ||||
| chr4:99088048-99088448 | Common:2; Rare:146 | ||||
| chr4:99088517-99089330 | Common:56; Rare:941 | ||||
| chr4:99562974-99563940 | Common:16; Rare:609 | ||||
| chr4:99563899-99564299 | Common:8; Rare:334; Clinvar:12; Clinvar (benign):8 | ||||
| chr4:99816559-99817600 | Common:12; Rare:365 | ||||
| chr4:99894280-99894920 | Common:15; Rare:532 | ||||
| chr4:99945877-99946586 | Common:4; Rare:238 | ||||
| chr4:99946534-99946813 | Rare:312 | ||||
| chr4:99946795-99947571 | Common:6; Rare:208 | ||||
| chr4:99949386-99950122 | Common:19; Rare:649 | ||||
| chr4:99950146-99950731 | Common:2; Rare:692 | ||||
| chr4:99950788-99951188 | Rare:80 |