| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941722-46941807 | Common:2; Rare:26 | ||||
| chr2:48314612-48314754 | Rare:56 | ||||
| chr2:48440626-48440966 | Common:7; Rare:148 | ||||
| chr2:53786923-53787169 | Common:1; Rare:99 | ||||
| chr2:53970774-53971163 | Common:12; Rare:144 | ||||
| chr2:55050342-55050763 | Common:5; Rare:126 | ||||
| chr2:55232245-55232385 | Common:2; Rare:33 | ||||
| chr2:55519452-55519804 | Common:1; Rare:107 | ||||
| chr2:58046771-58046836 | Rare:23 | ||||
| chr2:60881424-60881751 | Common:3; Rare:100 | ||||
| chr2:61017420-61017753 | Common:1; Rare:100; Clinvar:2 | ||||
| chr2:61144942-61145165 | Common:3; Rare:75 | ||||
| chr2:61854037-61854067 | Common:1; Rare:9; Clinvar:1 | ||||
| chr2:61888547-61888707 | Common:1; Rare:66 |