| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1013367-1013514 | Common:3; Rare:44 | ||||
| chr1:1324600-1324906 | Common:3; Rare:151 | ||||
| chr1:1658938-1659051 | Common:1; Rare:42 | ||||
| chr1:1724313-1724419 | Common:2; Rare:33 | ||||
| chr1:2391540-2391870 | Common:2; Rare:122 | ||||
| chr1:3772456-3772771 | Common:3; Rare:72 | ||||
| chr1:5992394-5992695 | Common:4; Rare:101; Clinvar:6 | ||||
| chr1:6208680-6208925 | Common:1; Rare:72 | ||||
| chr1:7961489-7961767 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:8878578-8878835 | Rare:130 | ||||
| chr1:9687536-9687688 | Common:2; Rare:35 | ||||
| chr1:9943318-9943488 | Common:2; Rare:38 | ||||
| chr1:10032763-10032959 | Rare:51 | ||||
| chr1:11654669-11654904 | Common:4; Rare:66 | ||||
| chr1:11805935-11806255 | Common:2; Rare:86; Clinvar:1 |