| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201643449-201643550 | Rare:29; Clinvar:3 | ||||
| chr2:201780896-201781249 | Common:3; Rare:109; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238634 | Rare:66; Clinvar:1 | ||||
| chr2:202634705-202635012 | Common:5; Rare:105 | ||||
| chr2:202870753-202870842 | Common:2; Rare:16 | ||||
| chr2:202870992-202871094 | Rare:23 | ||||
| chr2:202871205-202871372 | Common:1; Rare:42 | ||||
| chr2:202871419-202871816 | Common:4; Rare:128 | ||||
| chr2:202911606-202911716 | Rare:22 | ||||
| chr2:202911857-202912298 | Common:2; Rare:118 | ||||
| chr2:203014552-203014629 | Rare:27 | ||||
| chr2:203014649-203014920 | Common:1; Rare:80 | ||||
| chr2:203238680-203239047 | Common:2; Rare:109 | ||||
| chr2:203239227-203239358 | Rare:47 | ||||
| chr2:203328179-203328526 | Common:2; Rare:124 |