| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:25430153-25430344 | Common:8; Rare:123 | ||||
| chr1:25430644-25431082 | Common:4; Rare:134 | ||||
| chr1:25549480-25549930 | Common:12; Rare:153 | ||||
| chr1:25799901-25800241 | Common:1; Rare:169; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr1:25819802-25820037 | Common:8; Rare:127 | ||||
| chr1:25820740-25821350 | Common:11; Rare:186 | ||||
| chr1:25859344-25859609 | Common:6; Rare:214 | ||||
| chr1:25997936-25998451 | Common:6; Rare:220 | ||||
| chr1:26021638-26021803 | Common:1; Rare:28 | ||||
| chr1:26110860-26111205 | Common:4; Rare:134 | ||||
| chr1:26111450-26111990 | Common:4; Rare:228 | ||||
| chr1:26177395-26177563 | Common:4; Rare:89 | ||||
| chr1:26234350-26234660 | Common:4; Rare:155 | ||||
| chr1:26279769-26280153 | Common:1; Rare:288 | ||||
| chr1:26306570-26306860 | Common:26; Rare:162 |