| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226406524-226406872 | Common:3; Rare:62 | ||||
| chr1:226602596-226602971 | Common:3; Rare:74 | ||||
| chr1:226603440-226603499 | Rare:9 | ||||
| chr1:226702823-226703075 | Rare:41 | ||||
| chr1:226703287-226703449 | Common:1; Rare:50 | ||||
| chr1:226703460-226703726 | Common:2; Rare:95 | ||||
| chr1:226703789-226703793 | Common:1 | ||||
| chr1:226708540-226708668 | Rare:35 | ||||
| chr1:226738178-226738316 | Common:1; Rare:29 | ||||
| chr1:226778708-226778880 | Common:1; Rare:28 | ||||
| chr1:226815119-226815221 | Common:2; Rare:23 | ||||
| chr1:226821401-226821465 | Common:1; Rare:8 | ||||
| chr1:226863574-226863683 | Common:1; Rare:14 | ||||
| chr1:226982078-226982146 | Rare:25; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:226985399-226985492 | Rare:21 |