| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:212858089-212858289 | Common:3; Rare:50; Clinvar:1 | ||||
| chr1:212950383-212950655 | Common:2; Rare:71 | ||||
| chr1:213015443-213015545 | Rare:24 | ||||
| chr1:213051217-213051486 | Common:1; Rare:102 | ||||
| chr1:213987665-213987973 | Rare:57 | ||||
| chr1:214280952-214281266 | Common:2; Rare:130 | ||||
| chr1:214551552-214551932 | Common:2; Rare:121 | ||||
| chr1:214602855-214603299 | Common:3; Rare:124 | ||||
| chr1:217630924-217631418 | Common:4; Rare:150 | ||||
| chr1:217737700-217737844 | Common:1; Rare:23 | ||||
| chr1:218285143-218285449 | Common:5; Rare:122 | ||||
| chr1:218346688-218346825 | Rare:36; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:219173748-219173938 | Common:1; Rare:106 | ||||
| chr1:220046393-220046533 | Common:1; Rare:52 | ||||
| chr1:220272341-220272528 | Rare:49; Clinvar:5 |