| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170743954-170744047 | Rare:19 | ||||
| chr2:170751593-170751724 | Common:1; Rare:18 | ||||
| chr2:170770790-170771101 | Common:2; Rare:53 | ||||
| chr2:181461007-181461161 | Rare:27 | ||||
| chr2:188997170-188997371 | Common:4; Rare:47; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr2:189575144-189575442 | Rare:71; Clinvar (benign):1 | ||||
| chr2:200695697-200695917 | Common:1; Rare:31 | ||||
| chr2:202184604-202184794 | Common:1; Rare:43 | ||||
| chr2:203534430-203534565 | Common:4; Rare:23 | ||||
| chr2:210540172-210540278 | Common:1; Rare:25 | ||||
| chr2:215433582-215433833 | Common:1; Rare:54 | ||||
| chr2:216594190-216594421 | Rare:35 | ||||
| chr2:217840648-217840986 | Common:3; Rare:62 | ||||
| chr2:218402615-218402714 | Rare:37 | ||||
| chr2:218814616-218814951 | Rare:113; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):7 |