| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109409179-109409458 | Common:3; Rare:102 | ||||
| chr5:109409626-109410018 | Common:4; Rare:127 | ||||
| chr5:109689236-109689446 | Common:4; Rare:100 | ||||
| chr5:109689827-109690004 | Common:2; Rare:67 | ||||
| chr5:110738929-110739111 | Common:2; Rare:79 | ||||
| chr5:111092231-111092442 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111512384-111512875 | Common:4; Rare:153 | ||||
| chr5:111513036-111513278 | Common:1; Rare:47 | ||||
| chr5:111757173-111757218 | Rare:4 | ||||
| chr5:111757220-111757327 | Common:5; Rare:27 | ||||
| chr5:111757580-111757884 | Common:1; Rare:125 | ||||
| chr5:112707406-112707665 | Common:6; Rare:115; Clinvar:62; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr5:112861137-112861417 | Common:5; Rare:111 | ||||
| chr5:112862190-112862412 | Common:5; Rare:53 | ||||
| chr5:112921542-112921582 | Common:2; Rare:11 |