| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:2412498-2412837 | Common:2; Rare:274; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr1:2526086-2526486 | Common:3; Rare:193 | ||||
| chr1:2526401-2527043 | Common:8; Rare:264 | ||||
| chr1:2586260-2586520 | Common:2; Rare:104 | ||||
| chr1:3454064-3454785 | Common:2; Rare:302 | ||||
| chr1:3531315-3531609 | Common:4; Rare:162 | ||||
| chr1:3624719-3625088 | Common:2; Rare:222 | ||||
| chr1:3796463-3796612 | Common:4; Rare:98 | ||||
| chr1:3857133-3857513 | Common:4; Rare:202 | ||||
| chr1:3900054-3900478 | Common:24; Rare:264 | ||||
| chr1:5992341-5992763 | Common:8; Rare:247; Clinvar:10 | ||||
| chr1:6026132-6026397 | Common:1; Rare:51 | ||||
| chr1:6199515-6199692 | Rare:115 | ||||
| chr1:6199747-6200030 | Common:1; Rare:47 | ||||
| chr1:6206007-6206470 | Common:5; Rare:209 |