| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112231294-112231911 | Common:4; Rare:171 | ||||
| chr4:112232076-112232311 | Common:1; Rare:90 | ||||
| chr4:112285152-112285247 | Rare:19 | ||||
| chr4:112285717-112286072 | Common:1; Rare:101 | ||||
| chr4:112297216-112297412 | Common:1; Rare:33 | ||||
| chr4:112515570-112515881 | Common:2; Rare:66 | ||||
| chr4:112516515-112516723 | Common:1; Rare:54 | ||||
| chr4:112636892-112637213 | Common:2; Rare:86 | ||||
| chr4:112637384-112637578 | Common:3; Rare:54 | ||||
| chr4:112817976-112818182 | Rare:26 | ||||
| chr4:113355644-113355967 | Common:2; Rare:97; Clinvar:16; Clinvar (benign):13 | ||||
| chr4:113760229-113760745 | Common:2; Rare:110 | ||||
| chr4:113761109-113761306 | Common:1; Rare:47 | ||||
| chr4:113761574-113762010 | Common:2; Rare:117 | ||||
| chr4:113762014-113762398 | Common:1; Rare:91 |