| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88866188-88866322 | Common:3; Rare:33 | ||||
| chr2:88947788-88947853 | Common:1; Rare:38 | ||||
| chr2:88966756-88966881 | Rare:39 | ||||
| chr2:89320111-89320232 | Common:3; Rare:35 | ||||
| chr2:89585573-89585763 | Rare:1 | ||||
| chr2:91659919-91660047 | Rare:22 | ||||
| chr2:95526711-95526798 | Common:1; Rare:26 | ||||
| chr2:96761687-96762089 | Rare:96; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr2:97762160-97762386 | Rare:43 | ||||
| chr2:100818678-100818746 | Rare:12 | ||||
| chr2:101010933-101011131 | Rare:44 | ||||
| chr2:101014773-101015072 | Common:5; Rare:55 | ||||
| chr2:101020904-101021033 | Rare:26 | ||||
| chr2:101021697-101021846 | Rare:36 | ||||
| chr2:101034782-101035059 | Common:3; Rare:47 |