| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237475071-237475675 | Common:10; Rare:332 | ||||
| chr2:237475964-237476131 | Rare:33 | ||||
| chr2:237476315-237477453 | Common:14; Rare:241 | ||||
| chr2:237482500-237483455 | Common:16; Rare:374 | ||||
| chr2:237483398-237483738 | Common:8; Rare:123 | ||||
| chr2:237483938-237484357 | Common:21; Rare:248 | ||||
| chr2:237488207-237489431 | Common:30; Rare:569 | ||||
| chr2:237489364-237489870 | Common:13; Rare:204 | ||||
| chr2:237490152-237490601 | Common:11; Rare:160 | ||||
| chr2:237493400-237493814 | Common:1; Rare:99; Clinvar (pathogenic):2 | ||||
| chr2:237494090-237495186 | Common:10; Rare:352 | ||||
| chr2:237502141-237502377 | Common:7; Rare:45 | ||||
| chr2:237502460-237502848 | Common:14; Rare:125 | ||||
| chr2:237502794-237503050 | Common:6; Rare:38 | ||||
| chr2:237535526-237535915 | Common:3; Rare:69 |