| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108381320-108381526 | Common:1; Rare:68 | ||||
| chr5:108382063-108382179 | Common:1; Rare:44 | ||||
| chr5:108748645-108748991 | Common:2; Rare:121 | ||||
| chr5:109409096-109409115 | Rare:4 | ||||
| chr5:109409776-109410297 | Common:4; Rare:179 | ||||
| chr5:109689821-109690149 | Common:3; Rare:106 | ||||
| chr5:110738906-110739135 | Common:2; Rare:95; Clinvar (pathogenic):1 | ||||
| chr5:111512425-111512856 | Common:4; Rare:143 | ||||
| chr5:112419156-112419405 | Common:3; Rare:96 | ||||
| chr5:112707371-112707661 | Common:8; Rare:128; Clinvar:68; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr5:112737727-112737924 | Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:112861108-112861388 | Common:5; Rare:110 | ||||
| chr5:112921534-112921582 | Common:2; Rare:14 | ||||
| chr5:112922167-112922469 | Common:2; Rare:122 | ||||
| chr5:112976453-112976763 | Common:1; Rare:113 |