| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169746-42170346 | Common:2; Rare:261 | ||||
| chr2:42361510-42361712 | Common:1; Rare:75 | ||||
| chr2:42493966-42494066 | Rare:46 | ||||
| chr2:42567750-42568150 | Common:1; Rare:173 | ||||
| chr2:42568354-42568725 | Common:6; Rare:91 | ||||
| chr2:42569107-42569566 | Common:2; Rare:138 | ||||
| chr2:43225457-43226363 | Common:8; Rare:545 | ||||
| chr2:43226586-43226917 | Common:3; Rare:125 | ||||
| chr2:43595940-43596223 | Common:1; Rare:103 | ||||
| chr2:43637030-43637310 | Common:2; Rare:91 | ||||
| chr2:43773830-43774270 | Common:7; Rare:161; Clinvar (pathogenic):1 | ||||
| chr2:43995946-43996476 | Common:5; Rare:233; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44167890-44168260 | Common:4; Rare:142 | ||||
| chr2:44168901-44169768 | Common:4; Rare:415 | ||||
| chr2:44361464-44362018 | Common:4; Rare:178 |