| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231039274-231039458 | Common:1; Rare:56 | ||||
| chr1:231200431-231200607 | Rare:39 | ||||
| chr1:231211583-231211783 | Common:2; Rare:46 | ||||
| chr1:231233928-231234183 | Common:1; Rare:38 | ||||
| chr1:231234190-231234511 | Rare:56 | ||||
| chr1:231234569-231234727 | Rare:28 | ||||
| chr1:231395485-231395735 | Common:3; Rare:42 | ||||
| chr1:231420878-231420933 | Rare:16 | ||||
| chr1:231421866-231421907 | Rare:11; Clinvar (benign):1 | ||||
| chr1:231422216-231422541 | Common:6; Rare:144; Clinvar:5; Clinvar (benign):6 | ||||
| chr1:231422557-231422715 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:231627467-231627546 | Rare:13 | ||||
| chr1:231628263-231628574 | Common:1; Rare:47 | ||||
| chr1:231836595-231836840 | Common:4; Rare:56 | ||||
| chr1:232260701-232260794 | Rare:16 |