| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:88832681-88832866 | Rare:29 | ||||
| chr1:88832869-88833114 | Rare:44 | ||||
| chr1:88992588-88992988 | Common:3; Rare:104 | ||||
| chr1:89011884-89012160 | Common:1; Rare:66 | ||||
| chr1:89022685-89022908 | Rare:38 | ||||
| chr1:89065179-89065440 | Common:1; Rare:41 | ||||
| chr1:89125919-89126169 | Rare:53 | ||||
| chr1:89198845-89199012 | Common:1; Rare:28 | ||||
| chr1:89632887-89633189 | Common:1; Rare:83 | ||||
| chr1:89821029-89821222 | Common:1; Rare:61 | ||||
| chr1:89994981-89995232 | Common:2; Rare:94 | ||||
| chr1:91021963-91022409 | Common:1; Rare:108 | ||||
| chr1:91500568-91500890 | Common:3; Rare:79 | ||||
| chr1:91886006-91886348 | Rare:137 | ||||
| chr1:92298939-92299089 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 |