| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162073980-162074014 | Rare:15 | ||||
| chr2:162318446-162318811 | Common:2; Rare:73 | ||||
| chr2:162344311-162344387 | Rare:26 | ||||
| chr2:163735885-163736064 | Common:1; Rare:27 | ||||
| chr2:164840308-164840820 | Common:2; Rare:86 | ||||
| chr2:164841074-164841299 | Rare:58 | ||||
| chr2:164841717-164841977 | Common:1; Rare:69 | ||||
| chr2:164842143-164842257 | Common:1; Rare:21 | ||||
| chr2:164937904-164938257 | Common:2; Rare:52 | ||||
| chr2:164955308-164955615 | Rare:65 | ||||
| chr2:165469538-165469717 | Rare:34 | ||||
| chr2:165794085-165794395 | Common:2; Rare:86; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794680-165794842 | Common:1; Rare:29 | ||||
| chr2:165795141-165795233 | Rare:8 | ||||
| chr2:165871074-165871215 | Rare:29 |