| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229273790-229274260 | Common:8; Rare:120 | ||||
| chr1:230202851-230203500 | Common:2; Rare:286 | ||||
| chr1:230703132-230703532 | Rare:207; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr1:230708529-230708982 | Common:9; Rare:238 | ||||
| chr1:231422219-231422490 | Common:10; Rare:221; Clinvar:9; Clinvar (benign):10 | ||||
| chr1:234356737-234357044 | Common:4; Rare:129 | ||||
| chr1:234599650-234600390 | Common:19; Rare:343 | ||||
| chr1:234600586-234600755 | Rare:37 | ||||
| chr1:234610098-234610338 | Common:4; Rare:212 | ||||
| chr1:234610784-234611225 | Common:5; Rare:287 | ||||
| chr1:234611770-234612290 | Common:4; Rare:134 | ||||
| chr1:234612691-234612948 | Common:1; Rare:61 | ||||
| chr1:234619872-234620043 | Common:2; Rare:31 | ||||
| chr1:234620830-234621390 | Common:1; Rare:137 | ||||
| chr1:234624266-234624688 | Common:4; Rare:97 |