| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241149434-241149686 | Common:4; Rare:86 | ||||
| chr2:241315178-241315463 | Common:5; Rare:93 | ||||
| chr2:241315656-241315985 | Common:5; Rare:130 | ||||
| chr2:241637071-241637321 | Common:1; Rare:88 | ||||
| chr2:241637563-241637710 | Common:1; Rare:84 | ||||
| chr2:241686683-241687117 | Common:4; Rare:145 | ||||
| chr20:348158-348276 | Common:1; Rare:27 | ||||
| chr20:1118443-1118828 | Common:5; Rare:133 | ||||
| chr20:1894253-1894558 | Common:2; Rare:77 | ||||
| chr20:2652458-2652662 | Common:8; Rare:70 | ||||
| chr20:2840635-2840756 | Common:1; Rare:44 | ||||
| chr20:3801554-3801796 | Common:2; Rare:46 | ||||
| chr20:3889155-3889396 | Common:1; Rare:126; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:3889688-3889867 | Common:6; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:4686294-4686466 | Rare:42 |