| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181540-130181733 | Common:3; Rare:82 | ||||
| chr2:130182063-130182366 | Common:2; Rare:117 | ||||
| chr2:130342077-130342279 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342683-130342938 | Common:3; Rare:83 | ||||
| chr2:130355879-130356074 | Common:2; Rare:51 | ||||
| chr2:130372530-130372717 | Rare:57 | ||||
| chr2:130756025-130756902 | Common:6; Rare:300 | ||||
| chr2:130836680-130837100 | Common:4; Rare:128 | ||||
| chr2:130837205-130838041 | Common:5; Rare:249 | ||||
| chr2:131093388-131093614 | Common:1; Rare:106 | ||||
| chr2:131104936-131105365 | Common:3; Rare:136 | ||||
| chr2:131491265-131491665 | Common:3; Rare:92 | ||||
| chr2:131492378-131492588 | Common:6; Rare:77 | ||||
| chr2:131492650-131492940 | Common:5; Rare:84 | ||||
| chr2:131527680-131528174 | Common:10; Rare:224 |