| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11533280-11534776 | Common:20; Rare:405 | ||||
| chr2:11539366-11539888 | Common:5; Rare:128 | ||||
| chr2:11541799-11542860 | Common:18; Rare:331 | ||||
| chr2:11542941-11543882 | Common:18; Rare:156 | ||||
| chr2:11746476-11746763 | Common:6; Rare:215; Clinvar:14 | ||||
| chr2:12716549-12717072 | Common:9; Rare:369 | ||||
| chr2:14632493-14632874 | Common:3; Rare:288 | ||||
| chr2:15561240-15561470 | Rare:166 | ||||
| chr2:15591228-15592310 | Common:24; Rare:672 | ||||
| chr2:15592237-15592344 | Common:1; Rare:25 | ||||
| chr2:15940220-15940680 | Common:1; Rare:293 | ||||
| chr2:16665610-16666166 | Common:11; Rare:150 | ||||
| chr2:17518250-17518700 | Common:5; Rare:159 | ||||
| chr2:17753257-17753439 | Common:6; Rare:46 | ||||
| chr2:17753709-17754784 | Common:23; Rare:557; Clinvar (benign):3 |