| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:186828623-186829020 | Common:2; Rare:102 | ||||
| chr1:186829284-186829388 | Rare:16 | ||||
| chr1:192575531-192575873 | Common:3; Rare:81 | ||||
| chr1:192808600-192809127 | Common:5; Rare:188 | ||||
| chr1:193058535-193058796 | Common:2; Rare:54 | ||||
| chr1:193059249-193059741 | Common:1; Rare:230 | ||||
| chr1:193059991-193060090 | Rare:33 | ||||
| chr1:193105082-193105218 | Common:1; Rare:25 | ||||
| chr1:193105332-193105638 | Common:3; Rare:132 | ||||
| chr1:193121643-193121917 | Common:2; Rare:105 | ||||
| chr1:193121929-193122491 | Common:1; Rare:184; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr1:197146139-197146260 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:197146397-197146465 | Rare:27; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:197146585-197146902 | Rare:90; Clinvar:3 | ||||
| chr1:197902551-197902669 | Common:1; Rare:40 |