| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231529220-231529302 | Rare:33 | ||||
| chr1:232805207-232805452 | Common:3; Rare:132 | ||||
| chr1:232950453-232950669 | Common:3; Rare:79 | ||||
| chr1:233177350-233177432 | Common:2; Rare:9 | ||||
| chr1:233613470-233613645 | Common:1; Rare:44 | ||||
| chr1:234373311-234373775 | Common:1; Rare:210; Clinvar (benign):7 | ||||
| chr1:235128707-235128981 | Rare:119 | ||||
| chr1:235161004-235161348 | Common:2; Rare:184 | ||||
| chr1:235327280-235327387 | Rare:35 | ||||
| chr1:235328151-235328648 | Common:4; Rare:154 | ||||
| chr1:235328813-235328963 | Rare:53 | ||||
| chr1:235329271-235329557 | Rare:59 | ||||
| chr1:235866844-235867177 | Common:3; Rare:103 | ||||
| chr1:236065037-236065288 | Common:2; Rare:102; Clinvar (pathogenic):1 | ||||
| chr1:236281825-236282092 | Common:4; Rare:79 |