| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260420-201260590 | Rare:37 | ||||
| chr2:201451435-201451838 | Common:2; Rare:102 | ||||
| chr2:201642637-201642811 | Rare:78 | ||||
| chr2:201643435-201643562 | Rare:36; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:201780884-201781231 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238632 | Rare:66; Clinvar:1 | ||||
| chr2:202265669-202265888 | Rare:77 | ||||
| chr2:202634795-202635012 | Common:4; Rare:83 | ||||
| chr2:202871416-202871800 | Common:4; Rare:124 | ||||
| chr2:202911595-202911744 | Rare:26 | ||||
| chr2:202911832-202912298 | Common:2; Rare:124 | ||||
| chr2:202912474-202912571 | Common:2; Rare:32 | ||||
| chr2:203014506-203014944 | Common:1; Rare:141 | ||||
| chr2:203238887-203239068 | Common:2; Rare:76 | ||||
| chr2:203239183-203239338 | Rare:48 |