| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:67430303-67430596 | Rare:234 | ||||
| chr1:67430730-67430990 | Common:1; Rare:102 | ||||
| chr1:67684929-67685266 | Common:5; Rare:180 | ||||
| chr1:67833339-67833504 | Common:4; Rare:123 | ||||
| chr1:68232407-68232633 | Common:1; Rare:49 | ||||
| chr1:68497011-68497329 | Common:4; Rare:165 | ||||
| chr1:70205510-70205788 | Rare:168 | ||||
| chr1:70221282-70221709 | Rare:271 | ||||
| chr1:70354295-70354481 | Common:2; Rare:126 | ||||
| chr1:70354650-70354878 | Rare:140 | ||||
| chr1:70354910-70355220 | Common:3; Rare:201 | ||||
| chr1:70411053-70411323 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:71080960-71081398 | Rare:232 | ||||
| chr1:72282490-72283371 | Common:17; Rare:375 | ||||
| chr1:74198104-74198343 | Common:5; Rare:214 |