| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:224131128-224131218 | Common:1; Rare:13 | ||||
| chr1:224934900-224935120 | Common:2; Rare:36 | ||||
| chr1:225651433-225651563 | Common:1; Rare:21 | ||||
| chr1:225700307-225700649 | Common:2; Rare:51 | ||||
| chr1:225981597-225981622 | Common:1; Rare:3 | ||||
| chr1:226069212-226069322 | Rare:28 | ||||
| chr1:226083502-226083639 | Common:3; Rare:46 | ||||
| chr1:226984351-226984590 | Common:1; Rare:73; Clinvar (benign):4 | ||||
| chr1:229930901-229931193 | Common:1; Rare:38 | ||||
| chr1:231335038-231335164 | Rare:26 | ||||
| chr1:231366449-231366593 | Common:8; Rare:35; Clinvar (benign):1 | ||||
| chr1:231395529-231395732 | Common:3; Rare:34 | ||||
| chr1:231396064-231396240 | Common:1; Rare:37 | ||||
| chr1:231420998-231421523 | Common:2; Rare:169; Clinvar:6; Clinvar (benign):5 | ||||
| chr1:231422236-231422446 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):5 |