| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46303093-46303745 | Common:6; Rare:370 | ||||
| chr1:46340607-46340851 | Common:6; Rare:130 | ||||
| chr1:46604196-46604485 | Common:2; Rare:148 | ||||
| chr1:46616787-46616936 | Common:4; Rare:73 | ||||
| chr1:46668320-46668513 | Rare:115 | ||||
| chr1:46719025-46719322 | Common:1; Rare:195 | ||||
| chr1:47314019-47314549 | Common:9; Rare:235; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:47333703-47333988 | Common:6; Rare:184 | ||||
| chr1:47334160-47334350 | Common:3; Rare:102 | ||||
| chr1:47997354-47997487 | Rare:15 | ||||
| chr1:48472040-48472500 | Common:11; Rare:214 | ||||
| chr1:50423510-50424260 | Common:7; Rare:217 | ||||
| chr1:50959220-50959372 | Common:2; Rare:26 | ||||
| chr1:50959555-50959963 | Common:4; Rare:168 | ||||
| chr1:50960046-50960413 | Rare:202 |