| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:153986259-153986532 | Common:1; Rare:105 | ||||
| chr1:153990583-153990883 | Common:6; Rare:321 | ||||
| chr1:154182371-154182870 | Common:1; Rare:179 | ||||
| chr1:154183141-154183543 | Rare:243 | ||||
| chr1:154193790-154194190 | Common:1; Rare:77 | ||||
| chr1:154220127-154220423 | Rare:167 | ||||
| chr1:154220441-154221372 | Common:3; Rare:675 | ||||
| chr1:154272359-154272770 | Common:13; Rare:243; Clinvar:6; Clinvar (benign):9 | ||||
| chr1:154272902-154273715 | Common:13; Rare:370; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr1:154325262-154325908 | Common:1; Rare:295 | ||||
| chr1:154328360-154329070 | Common:9; Rare:391 | ||||
| chr1:154404851-154405646 | Common:7; Rare:288 | ||||
| chr1:154558583-154559119 | Common:6; Rare:455 | ||||
| chr1:154567386-154567949 | Common:7; Rare:186 | ||||
| chr1:154607025-154607857 | Common:18; Rare:262 |