| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:95117211-95117448 | Rare:74 | ||||
| chr1:95233945-95234236 | Common:8; Rare:161 | ||||
| chr1:96721596-96721864 | Common:4; Rare:238 | ||||
| chr1:97920889-97921261 | Common:2; Rare:128; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr1:98661461-98661879 | Common:6; Rare:240 | ||||
| chr1:98662030-98662330 | Rare:105 | ||||
| chr1:99645861-99646135 | Rare:48 | ||||
| chr1:99646100-99646241 | Rare:35 | ||||
| chr1:99850004-99850199 | Common:2; Rare:134 | ||||
| chr1:99969480-99969737 | Common:1; Rare:68 | ||||
| chr1:99969879-99970115 | Rare:101 | ||||
| chr1:100037968-100038244 | Common:2; Rare:180 | ||||
| chr1:100132881-100133212 | Common:6; Rare:219 | ||||
| chr1:100266089-100266327 | Common:5; Rare:166 | ||||
| chr1:100351550-100351950 | Common:6; Rare:199 |