| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47345064-47345334 | Common:1; Rare:76 | ||||
| chr2:47369151-47369586 | Common:4; Rare:185; Clinvar:18; Clinvar (benign):6 | ||||
| chr2:47402945-47403187 | Common:1; Rare:110; Clinvar:33; Clinvar (benign):26 | ||||
| chr2:47905489-47905819 | Common:3; Rare:158 | ||||
| chr2:48440621-48440858 | Common:8; Rare:113 | ||||
| chr2:53767559-53767849 | Common:4; Rare:101 | ||||
| chr2:53786862-53787191 | Common:1; Rare:125 | ||||
| chr2:53970780-53971204 | Common:12; Rare:153 | ||||
| chr2:54115423-54115701 | Rare:93 | ||||
| chr2:54558064-54558582 | Common:5; Rare:155 | ||||
| chr2:54558680-54558879 | Common:1; Rare:64 | ||||
| chr2:55050267-55050763 | Common:5; Rare:163 | ||||
| chr2:55232235-55232719 | Common:4; Rare:131 | ||||
| chr2:55269157-55269303 | Common:2; Rare:43 | ||||
| chr2:55519425-55519794 | Common:1; Rare:111 |