| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73926064-73926464 | Common:3; Rare:70 | ||||
| chr2:73926668-73927083 | Common:14; Rare:937; Clinvar:55; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr2:73985611-73986130 | Common:11; Rare:266 | ||||
| chr2:74002480-74002780 | Common:6; Rare:215 | ||||
| chr2:74146901-74147696 | Common:3; Rare:337 | ||||
| chr2:74147822-74148222 | Common:17; Rare:581; Clinvar:14; Clinvar (benign):8 | ||||
| chr2:74148194-74149062 | Common:9; Rare:320 | ||||
| chr2:74178090-74178620 | Rare:201 | ||||
| chr2:74178703-74179173 | Common:27; Rare:633 | ||||
| chr2:74198290-74198674 | Common:17; Rare:716 | ||||
| chr2:74198826-74199464 | Common:7; Rare:408 | ||||
| chr2:74391505-74392332 | Common:17; Rare:1085 | ||||
| chr2:74421485-74421893 | Rare:471 | ||||
| chr2:74421998-74422398 | Rare:194 | ||||
| chr2:74440305-74440790 | Common:1; Rare:285 |