| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96870765-96870850 | Rare:14 | ||||
| chr2:97094829-97094925 | Common:1; Rare:20 | ||||
| chr2:97589707-97589909 | Common:6; Rare:54 | ||||
| chr2:97589912-97590040 | Common:1; Rare:32 | ||||
| chr2:97645808-97646161 | Common:3; Rare:105 | ||||
| chr2:97663902-97664302 | Common:1; Rare:123 | ||||
| chr2:97713434-97713673 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:97995924-97995968 | Rare:20 | ||||
| chr2:98608320-98608659 | Common:1; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98663422-98663649 | Common:2; Rare:38 | ||||
| chr2:98731062-98731306 | Common:3; Rare:87 | ||||
| chr2:99141133-99141445 | Common:1; Rare:114 | ||||
| chr2:99141506-99141740 | Common:2; Rare:86 | ||||
| chr2:99154877-99155103 | Common:2; Rare:91; Clinvar (benign):3 | ||||
| chr2:99180853-99181226 | Common:2; Rare:122 |