| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40709158-40709392 | Rare:53 | ||||
| chr1:40862274-40862615 | Common:10; Rare:194 | ||||
| chr1:40979606-40979786 | Common:3; Rare:62 | ||||
| chr1:41241160-41241810 | Common:1; Rare:193 | ||||
| chr1:41242077-41242377 | Rare:158 | ||||
| chr1:42334942-42335437 | Common:13; Rare:349 | ||||
| chr1:42456424-42456632 | Common:1; Rare:149 | ||||
| chr1:42658295-42658502 | Common:2; Rare:107 | ||||
| chr1:42682102-42682584 | Common:4; Rare:218 | ||||
| chr1:42740001-42740820 | Common:5; Rare:225; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42766957-42767317 | Common:10; Rare:243; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:42816820-42817140 | Common:3; Rare:155 | ||||
| chr1:42817200-42817630 | Rare:219 | ||||
| chr1:42846381-42846657 | Common:2; Rare:151 | ||||
| chr1:42958635-42959115 | Common:8; Rare:225; Clinvar:12; Clinvar (benign):14 |