| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1013382-1013576 | Common:4; Rare:63 | ||||
| chr1:1047562-1047780 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):4 | ||||
| chr1:1324580-1324973 | Common:3; Rare:175 | ||||
| chr1:1375142-1375420 | Common:3; Rare:71 | ||||
| chr1:1399272-1399582 | Common:1; Rare:142 | ||||
| chr1:1574526-1574944 | Common:1; Rare:189 | ||||
| chr1:1658923-1659031 | Common:2; Rare:40 | ||||
| chr1:1692470-1692555 | Common:2; Rare:15 | ||||
| chr1:1724246-1724439 | Common:3; Rare:66 | ||||
| chr1:2391519-2391908 | Common:2; Rare:144 | ||||
| chr1:2556293-2556594 | Common:2; Rare:114 | ||||
| chr1:3857209-3857315 | Common:1; Rare:34 | ||||
| chr1:3900182-3900427 | Common:12; Rare:116 | ||||
| chr1:5992400-5992711 | Common:4; Rare:104; Clinvar:6 | ||||
| chr1:6205995-6206116 | Common:2; Rare:28 |