| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210476650-210476864 | Rare:132 | ||||
| chr2:210477580-210477699 | Rare:79 | ||||
| chr2:212538505-212539029 | Common:3; Rare:267 | ||||
| chr2:212538936-212539506 | Common:21; Rare:230 | ||||
| chr2:213150284-213150732 | Common:13; Rare:174 | ||||
| chr2:213151525-213152025 | Common:4; Rare:410 | ||||
| chr2:213152150-213152783 | Common:10; Rare:240 | ||||
| chr2:214808640-214809410 | Common:21; Rare:272; Clinvar (benign):2 | ||||
| chr2:214809546-214810310 | Common:48; Rare:912; Clinvar:11; Clinvar (benign):19 | ||||
| chr2:215137690-215138136 | Common:8; Rare:177 | ||||
| chr2:215138139-215138528 | Rare:105; Clinvar:1 | ||||
| chr2:215138472-215138965 | Common:6; Rare:230 | ||||
| chr2:215311801-215312380 | Common:28; Rare:561 | ||||
| chr2:215312651-215312953 | Common:2; Rare:69 | ||||
| chr2:215436020-215436350 | Common:4; Rare:175 |