| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:192809441-192809521 | Rare:13 | ||||
| chr1:193058673-193058960 | Common:3; Rare:55 | ||||
| chr1:193058982-193059089 | Common:1; Rare:24 | ||||
| chr1:193059153-193059809 | Common:2; Rare:282 | ||||
| chr1:193059837-193060247 | Common:1; Rare:140 | ||||
| chr1:193060553-193060626 | Rare:10 | ||||
| chr1:193104899-193105208 | Common:1; Rare:66 | ||||
| chr1:193105238-193105731 | Common:5; Rare:203 | ||||
| chr1:193121630-193122216 | Common:3; Rare:206; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:193122229-193122499 | Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:196608511-196608625 | Rare:29 | ||||
| chr1:196651890-196652083 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:197146140-197146278 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:197146354-197146488 | Rare:64; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr1:197146534-197146881 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):1 |