| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1341782-1342082 | Common:8; Rare:113 | ||||
| chr5:1799785-1799993 | Common:7; Rare:98 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422292-5422684 | Common:3; Rare:138 | ||||
| chr5:6378507-6378706 | Rare:74 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249842-10250167 | Common:16; Rare:156 | ||||
| chr5:10250187-10250398 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353553-10353901 | Common:4; Rare:134 | ||||
| chr5:14664572-14664664 | Common:2; Rare:39 | ||||
| chr5:16465709-16465902 | Rare:37 | ||||
| chr5:31532043-31532381 | Common:3; Rare:97 | ||||
| chr5:32174277-32174426 | Common:1; Rare:53 | ||||
| chr5:33440626-33441049 | Common:5; Rare:111 | ||||
| chr5:34915214-34915345 | Rare:37 |