| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40531497-40531721 | Common:1; Rare:60 | ||||
| chr1:40691497-40691862 | Common:3; Rare:164 | ||||
| chr1:40691999-40692290 | Common:2; Rare:93 | ||||
| chr1:40979495-40979865 | Common:4; Rare:125 | ||||
| chr1:40981046-40981078 | Rare:7 | ||||
| chr1:41242074-41242188 | Rare:28 | ||||
| chr1:42335118-42335320 | Common:2; Rare:99 | ||||
| chr1:42456229-42456597 | Common:1; Rare:118 | ||||
| chr1:42682215-42682424 | Common:2; Rare:53 | ||||
| chr1:42766506-42766813 | Rare:89; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:42766976-42767309 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr1:42816921-42817139 | Common:1; Rare:63 | ||||
| chr1:42817194-42817462 | Rare:95 | ||||
| chr1:42846392-42846650 | Common:1; Rare:72 | ||||
| chr1:42958646-42959048 | Common:3; Rare:102; Clinvar:5; Clinvar (benign):8 |