| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799111-1799511 | Common:10; Rare:167 | ||||
| chr5:1799691-1800158 | Common:50; Rare:801 | ||||
| chr5:1800198-1800908 | Common:8; Rare:202 | ||||
| chr5:1801110-1801707 | Common:27; Rare:923; Clinvar:21; Clinvar (benign):17 | ||||
| chr5:5422146-5422800 | Common:18; Rare:1160 | ||||
| chr5:6378427-6378827 | Common:1; Rare:636 | ||||
| chr5:6631933-6632654 | Common:6; Rare:216; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:6632910-6633570 | Common:52; Rare:968; Clinvar:58; Clinvar (benign):27 | ||||
| chr5:6633590-6633750 | Common:2; Rare:84 | ||||
| chr5:6712568-6713555 | Common:36; Rare:1037 | ||||
| chr5:7868897-7869297 | Common:15; Rare:945; Clinvar:2; Clinvar (benign):9 | ||||
| chr5:7869506-7869906 | Common:6; Rare:135 | ||||
| chr5:10249578-10250569 | Common:119; Rare:1973; Clinvar:31; Clinvar (benign):14 | ||||
| chr5:10250601-10251001 | Common:2; Rare:207 | ||||
| chr5:10257851-10258398 | Common:4; Rare:235; Clinvar:6; Clinvar (benign):1 |