| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1013358-1013526 | Common:3; Rare:50 | ||||
| chr1:1324600-1324835 | Common:3; Rare:128 | ||||
| chr1:1375240-1375611 | Common:7; Rare:112 | ||||
| chr1:1399312-1399582 | Common:1; Rare:119 | ||||
| chr1:1574536-1574963 | Common:1; Rare:198 | ||||
| chr1:1658935-1659039 | Common:1; Rare:37 | ||||
| chr1:1724285-1724425 | Common:2; Rare:46 | ||||
| chr1:1890868-1891197 | Rare:126 | ||||
| chr1:2391540-2391888 | Common:2; Rare:129 | ||||
| chr1:3900219-3900406 | Common:11; Rare:87 | ||||
| chr1:6206012-6206105 | Common:2; Rare:18 | ||||
| chr1:6208680-6208886 | Common:1; Rare:58 | ||||
| chr1:6385789-6385927 | Common:1; Rare:43 | ||||
| chr1:7954162-7954293 | Rare:38 | ||||
| chr1:7961419-7961792 | Common:4; Rare:130; Clinvar:3; Clinvar (benign):3 |