| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:87331574-87331779 | Rare:64 | ||||
| chr1:88684064-88684359 | Common:3; Rare:81 | ||||
| chr1:88891495-88891697 | Common:1; Rare:94 | ||||
| chr1:88992584-88993142 | Common:6; Rare:141 | ||||
| chr1:89198851-89199019 | Rare:25 | ||||
| chr1:89632887-89633194 | Common:1; Rare:85 | ||||
| chr1:89994981-89995218 | Common:2; Rare:89 | ||||
| chr1:91021464-91021668 | Common:2; Rare:47 | ||||
| chr1:91404800-91404841 | Rare:14 | ||||
| chr1:91500568-91500925 | Common:3; Rare:90 | ||||
| chr1:91885904-91886165 | Rare:96 | ||||
| chr1:91886173-91886333 | Rare:70 | ||||
| chr1:92298939-92299074 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92785066-92785382 | Common:6; Rare:102 | ||||
| chr1:92832000-92832113 | Rare:75; Clinvar:6; Clinvar (benign):5 |