| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:959172-959512 | Common:5; Rare:391 | ||||
| chr1:960481-960990 | Common:5; Rare:382 | ||||
| chr1:966394-966548 | Common:4; Rare:63 | ||||
| chr1:966923-967054 | Rare:58 | ||||
| chr1:966964-967074 | Rare:50 | ||||
| chr1:976470-976940 | Common:6; Rare:104 | ||||
| chr1:999969-1000548 | Common:20; Rare:373 | ||||
| chr1:1000612-1001012 | Common:8; Rare:166 | ||||
| chr1:1013304-1013647 | Common:17; Rare:327 | ||||
| chr1:1019412-1019675 | Common:4; Rare:192 | ||||
| chr1:1019724-1020341 | Common:7; Rare:308; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:1033560-1034165 | Common:2; Rare:203 | ||||
| chr1:1050692-1050965 | Common:3; Rare:110; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:1115906-1116327 | Common:1; Rare:170 | ||||
| chr1:1205557-1205957 | Common:2; Rare:99 |