| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113192982-113193276 | Rare:70 | ||||
| chr2:113542668-113542704 | Rare:6 | ||||
| chr2:113584021-113584120 | Rare:26 | ||||
| chr2:121203990-121204261 | Common:1; Rare:59 | ||||
| chr2:121529891-121530164 | Common:2; Rare:65 | ||||
| chr2:127050802-127050995 | Common:1; Rare:59; Clinvar:4 | ||||
| chr2:127057721-127057865 | Common:1; Rare:35 | ||||
| chr2:131681740-131681871 | Common:3; Rare:22 | ||||
| chr2:131682266-131682542 | Common:5; Rare:71 | ||||
| chr2:132347186-132347494 | Common:3; Rare:68 | ||||
| chr2:133266636-133266765 | Common:2; Rare:35 | ||||
| chr2:134372913-134373123 | Common:1; Rare:34 | ||||
| chr2:135162522-135162818 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:143718832-143719084 | Common:2; Rare:36 | ||||
| chr2:144488186-144488440 | Common:1; Rare:34 |