| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:94418215-94418481 | Common:2; Rare:94 | ||||
| chr1:94541720-94541992 | Rare:79 | ||||
| chr1:94820140-94820382 | Common:4; Rare:59 | ||||
| chr1:94925730-94925918 | Rare:34 | ||||
| chr1:94926930-94927019 | Common:1; Rare:23 | ||||
| chr1:95072857-95073027 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr1:95233945-95234231 | Common:5; Rare:83 | ||||
| chr1:96721610-96721871 | Common:2; Rare:123 | ||||
| chr1:98661602-98661879 | Common:2; Rare:99 | ||||
| chr1:99264225-99264579 | Common:2; Rare:112 | ||||
| chr1:99849997-99850393 | Common:1; Rare:109; Clinvar:2 | ||||
| chr1:99969853-99970129 | Common:1; Rare:63 | ||||
| chr1:100037973-100038188 | Common:1; Rare:84 | ||||
| chr1:100132895-100133224 | Common:2; Rare:126 | ||||
| chr1:100249803-100250017 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):1 |