| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109689804-109690074 | Common:4; Rare:181 | ||||
| chr5:110738925-110739070 | Common:3; Rare:100 | ||||
| chr5:110739320-110739770 | Common:10; Rare:216; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:111092106-111092439 | Common:4; Rare:254; Clinvar:4; Clinvar (benign):8 | ||||
| chr5:111512055-111512300 | Common:3; Rare:114 | ||||
| chr5:111512400-111512875 | Common:7; Rare:287 | ||||
| chr5:112419030-112419390 | Common:8; Rare:223 | ||||
| chr5:112419410-112419640 | Common:1; Rare:135 | ||||
| chr5:112419692-112419807 | Common:3; Rare:50 | ||||
| chr5:112707387-112707665 | Common:12; Rare:210; Clinvar:113; Clinvar (benign):24; Clinvar (pathogenic):2 | ||||
| chr5:112737766-112737900 | Rare:58; Clinvar (benign):4 | ||||
| chr5:112861102-112861391 | Common:8; Rare:185 | ||||
| chr5:112920980-112921340 | Common:3; Rare:179 | ||||
| chr5:112921360-112921850 | Common:7; Rare:185 | ||||
| chr5:112976550-112976881 | Common:2; Rare:157 |