| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235866852-235867132 | Common:3; Rare:82 | ||||
| chr1:236064991-236065367 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
| chr1:236281936-236282249 | Common:6; Rare:91 | ||||
| chr1:236523867-236524034 | Common:2; Rare:43 | ||||
| chr1:236524512-236524608 | Common:1; Rare:20 | ||||
| chr1:236795113-236795452 | Common:5; Rare:143; Clinvar:3 | ||||
| chr1:239719083-239719132 | Rare:3 | ||||
| chr1:241639634-241639871 | Common:3; Rare:58 | ||||
| chr1:241848099-241848232 | Common:1; Rare:29 | ||||
| chr1:243255045-243255344 | Common:1; Rare:66 | ||||
| chr1:243255776-243256113 | Rare:94; Clinvar:4 | ||||
| chr1:244048236-244048542 | Rare:96 | ||||
| chr1:244451789-244452225 | Common:1; Rare:147 | ||||
| chr1:244835016-244835333 | Rare:118 | ||||
| chr1:244835575-244835736 | Common:2; Rare:69; Clinvar (benign):4 |