| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599217-33599442 | Common:1; Rare:86 | ||||
| chr2:37084262-37084575 | Common:4; Rare:118 | ||||
| chr2:37196431-37196514 | Rare:25 | ||||
| chr2:37231491-37231769 | Common:6; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37671618-37671782 | Common:2; Rare:76 | ||||
| chr2:37672131-37672255 | Common:3; Rare:39 | ||||
| chr2:38377200-38377599 | Common:3; Rare:167 | ||||
| chr2:38602886-38603198 | Common:4; Rare:121 | ||||
| chr2:38751286-38751668 | Common:6; Rare:191 | ||||
| chr2:38875628-38876089 | Common:3; Rare:139 | ||||
| chr2:39120995-39121151 | Rare:60 | ||||
| chr2:39437078-39437465 | Common:4; Rare:139 | ||||
| chr2:40451592-40451797 | Common:4; Rare:67 | ||||
| chr2:40451927-40452241 | Common:4; Rare:105 | ||||
| chr2:42169148-42169423 | Common:1; Rare:138 |