| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854493-233854720 | Common:4; Rare:64 | ||||
| chr2:236569771-236569921 | Rare:34 | ||||
| chr2:237085803-237085951 | Common:1; Rare:60 | ||||
| chr2:237487150-237487283 | Common:2; Rare:34 | ||||
| chr2:240025292-240025446 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:241102259-241102395 | Common:2; Rare:50 | ||||
| chr2:241149450-241149606 | Common:1; Rare:49 | ||||
| chr2:241271929-241271997 | Rare:15 | ||||
| chr2:241272770-241272951 | Rare:70 | ||||
| chr2:241315114-241315406 | Common:5; Rare:99 | ||||
| chr2:241315649-241315981 | Common:5; Rare:129 | ||||
| chr2:241637531-241637704 | Common:1; Rare:95 | ||||
| chr2:241686779-241686973 | Rare:59 | ||||
| chr20:346942-347121 | Common:1; Rare:52 | ||||
| chr20:348145-348237 | Rare:25 |