| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:89363684-89363996 | Rare:49 | ||||
| chr1:89632921-89633196 | Common:1; Rare:78 | ||||
| chr1:89994981-89995165 | Common:2; Rare:74 | ||||
| chr1:91021963-91022214 | Rare:74 | ||||
| chr1:91500736-91500901 | Common:2; Rare:53 | ||||
| chr1:92298945-92299101 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92785066-92785376 | Common:6; Rare:101 | ||||
| chr1:93079067-93079308 | Common:3; Rare:102 | ||||
| chr1:93180204-93180754 | Common:2; Rare:217 | ||||
| chr1:93345777-93345962 | Common:4; Rare:72 | ||||
| chr1:93879137-93879274 | Common:1; Rare:47 | ||||
| chr1:94418133-94418470 | Common:2; Rare:120 | ||||
| chr1:94541537-94542000 | Common:1; Rare:136 | ||||
| chr1:94820269-94820413 | Common:2; Rare:43 | ||||
| chr1:95233955-95234233 | Common:5; Rare:83 |