| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1013382-1013528 | Common:3; Rare:43 | ||||
| chr1:1324613-1324813 | Common:2; Rare:110 | ||||
| chr1:1375249-1375617 | Common:7; Rare:111 | ||||
| chr1:1399312-1399575 | Common:1; Rare:113 | ||||
| chr1:1407203-1407355 | Common:1; Rare:70 | ||||
| chr1:1658941-1659060 | Common:1; Rare:46 | ||||
| chr1:1692450-1692571 | Common:2; Rare:20 | ||||
| chr1:1724280-1724440 | Common:3; Rare:55 | ||||
| chr1:2391532-2391868 | Common:2; Rare:122 | ||||
| chr1:3900219-3900352 | Common:10; Rare:66 | ||||
| chr1:6199545-6199809 | Common:2; Rare:85 | ||||
| chr1:6208680-6208851 | Common:1; Rare:45 | ||||
| chr1:6701784-6701983 | Rare:62 | ||||
| chr1:7771146-7771363 | Common:4; Rare:90 | ||||
| chr1:7961455-7961757 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):3 |