| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151346843-151347075 | Rare:63 | ||||
| chr1:151347131-151347556 | Rare:92 | ||||
| chr1:151399225-151399279 | Common:6; Rare:13 | ||||
| chr1:151399336-151399607 | Common:3; Rare:70; Clinvar (pathogenic):1 | ||||
| chr1:151399686-151399807 | Rare:27 | ||||
| chr1:151400076-151400205 | Common:1; Rare:38 | ||||
| chr1:151400907-151401023 | Common:1; Rare:17 | ||||
| chr1:151458499-151459274 | Common:8; Rare:331 | ||||
| chr1:151459301-151459825 | Common:2; Rare:167 | ||||
| chr1:151511155-151511417 | Common:4; Rare:61 | ||||
| chr1:151539479-151539933 | Common:2; Rare:58 | ||||
| chr1:151540103-151540623 | Common:2; Rare:149 | ||||
| chr1:151540707-151540798 | Common:1; Rare:22 | ||||
| chr1:151611848-151612290 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:151612337-151612468 | Rare:28; Clinvar (benign):1 |