| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197499788-197500431 | Common:2; Rare:244; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515780-197516107 | Common:2; Rare:113 | ||||
| chr2:199911052-199911426 | Rare:120 | ||||
| chr2:200306034-200306081 | Rare:8 | ||||
| chr2:200306420-200306907 | Common:4; Rare:144 | ||||
| chr2:200509896-200510221 | Common:2; Rare:111 | ||||
| chr2:200864232-200864252 | Rare:5 | ||||
| chr2:200864625-200864811 | Rare:71 | ||||
| chr2:200888992-200889448 | Common:3; Rare:143 | ||||
| chr2:200963587-200963897 | Common:1; Rare:79 | ||||
| chr2:201071626-201072058 | Rare:89 | ||||
| chr2:201451435-201451816 | Common:2; Rare:97 | ||||
| chr2:201642627-201642729 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr2:201643444-201643577 | Rare:34; Clinvar:3 | ||||
| chr2:202238447-202238687 | Common:1; Rare:85; Clinvar:1 |