| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120252536-120253082 | Common:9; Rare:452 | ||||
| chr2:120253160-120253350 | Common:3; Rare:117 | ||||
| chr2:120345910-120346527 | Common:14; Rare:361 | ||||
| chr2:121530231-121530475 | Common:2; Rare:161 | ||||
| chr2:121530534-121531311 | Common:35; Rare:867; Clinvar (pathogenic):19 | ||||
| chr2:121649372-121649830 | Common:7; Rare:309 | ||||
| chr2:121649872-121650205 | Common:3; Rare:217 | ||||
| chr2:121736766-121737317 | Common:15; Rare:458 | ||||
| chr2:121755348-121755825 | Common:17; Rare:418 | ||||
| chr2:121755792-121756192 | Rare:179 | ||||
| chr2:127107019-127107560 | Common:17; Rare:343; Clinvar:20; Clinvar (benign):3 | ||||
| chr2:127294040-127294295 | Common:6; Rare:222; Clinvar:4; Clinvar (benign):6 | ||||
| chr2:127387190-127387619 | Common:10; Rare:272 | ||||
| chr2:127387822-127388351 | Common:30; Rare:562 | ||||
| chr2:127526335-127526661 | Common:6; Rare:300 |