| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1013388-1013514 | Common:3; Rare:41 | ||||
| chr1:1324600-1324932 | Common:3; Rare:158 | ||||
| chr1:1331170-1331361 | Common:2; Rare:73 | ||||
| chr1:1375164-1375478 | Common:5; Rare:82 | ||||
| chr1:1399280-1399610 | Common:1; Rare:153 | ||||
| chr1:1407167-1407312 | Common:1; Rare:73 | ||||
| chr1:1658938-1659290 | Common:5; Rare:136 | ||||
| chr1:1724299-1724510 | Common:4; Rare:72 | ||||
| chr1:1780139-1780363 | Common:1; Rare:36 | ||||
| chr1:2391540-2391873 | Common:2; Rare:124 | ||||
| chr1:3857193-3857485 | Common:1; Rare:78 | ||||
| chr1:3900219-3900406 | Common:11; Rare:87 | ||||
| chr1:6026155-6026381 | Common:1; Rare:49 | ||||
| chr1:6625073-6625216 | Rare:57 | ||||
| chr1:7961455-7961767 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):3 |