| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:98773857-98774073 | Common:2; Rare:77 | ||||
| chr5:98928799-98929224 | Common:5; Rare:179 | ||||
| chr5:100535191-100535424 | Rare:58 | ||||
| chr5:100903157-100903423 | Common:1; Rare:52 | ||||
| chr5:102755000-102755326 | Common:3; Rare:106 | ||||
| chr5:102807982-102808240 | Common:2; Rare:58 | ||||
| chr5:103120082-103120482 | Common:1; Rare:102 | ||||
| chr5:103259243-103259433 | Common:1; Rare:70 | ||||
| chr5:103562532-103562585 | Rare:17 | ||||
| chr5:103562760-103562896 | Common:7; Rare:56 | ||||
| chr5:108380388-108380697 | Common:1; Rare:84 | ||||
| chr5:108381768-108382198 | Common:6; Rare:163 | ||||
| chr5:108748686-108748993 | Common:2; Rare:104 | ||||
| chr5:109409842-109410249 | Common:4; Rare:155 | ||||
| chr5:110738906-110739141 | Common:2; Rare:97; Clinvar (pathogenic):1 |