| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120223366-120223496 | Rare:39 | ||||
| chr2:121530595-121530949 | Common:7; Rare:203; Clinvar (pathogenic):12 | ||||
| chr2:121755387-121755720 | Common:3; Rare:104 | ||||
| chr2:127811150-127811312 | Common:1; Rare:57 | ||||
| chr2:127858029-127858224 | Common:2; Rare:96 | ||||
| chr2:128091054-128091347 | Common:8; Rare:98 | ||||
| chr2:130181561-130181714 | Common:1; Rare:58 | ||||
| chr2:130182089-130182279 | Common:1; Rare:68 | ||||
| chr2:130342123-130342249 | Rare:52; Clinvar:1 | ||||
| chr2:130342390-130342474 | Common:2; Rare:18 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 | ||||
| chr2:130372631-130372725 | Rare:33 | ||||
| chr2:131105214-131105365 | Common:1; Rare:68 | ||||
| chr2:131492826-131492947 | Common:2; Rare:29 | ||||
| chr2:131493015-131493136 | Common:1; Rare:35 |