| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:100903162-100903413 | Common:1; Rare:48 | ||||
| chr5:103120072-103120467 | Common:1; Rare:102 | ||||
| chr5:103562745-103562946 | Common:7; Rare:75 | ||||
| chr5:108748317-108748427 | Common:4; Rare:21 | ||||
| chr5:108748686-108748993 | Common:2; Rare:104 | ||||
| chr5:109408875-109409115 | Common:4; Rare:58 | ||||
| chr5:109409286-109409461 | Common:1; Rare:58 | ||||
| chr5:109409830-109410235 | Common:4; Rare:155 | ||||
| chr5:109689246-109689435 | Common:4; Rare:90 | ||||
| chr5:110738906-110739150 | Common:2; Rare:101; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:111512440-111512856 | Common:4; Rare:138 | ||||
| chr5:111756236-111756321 | Common:1; Rare:5 | ||||
| chr5:111757550-111757862 | Common:1; Rare:121 | ||||
| chr5:111757946-111758106 | Common:2; Rare:58 | ||||
| chr5:112707381-112707668 | Common:6; Rare:126; Clinvar:69; Clinvar (benign):12; Clinvar (pathogenic):1 |