| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73232780-73232897 | Rare:35 | ||||
| chr2:73233165-73233620 | Common:8; Rare:672 | ||||
| chr2:73233774-73234174 | Common:2; Rare:71 | ||||
| chr2:73234117-73234394 | Common:10; Rare:289 | ||||
| chr2:73234385-73234790 | Common:4; Rare:331 | ||||
| chr2:73283800-73284200 | Common:2; Rare:85 | ||||
| chr2:73284250-73285046 | Common:16; Rare:914 | ||||
| chr2:73385518-73386152 | Common:14; Rare:999; Clinvar:64; Clinvar (benign):30; Clinvar (pathogenic):4 | ||||
| chr2:73386100-73386490 | Common:4; Rare:313; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr2:73736594-73737204 | Common:6; Rare:213 | ||||
| chr2:73737180-73737671 | Common:13; Rare:519 | ||||
| chr2:73779414-73779900 | Rare:179 | ||||
| chr2:73780009-73780390 | Common:3; Rare:322 | ||||
| chr2:73828656-73829070 | Common:9; Rare:381 | ||||
| chr2:73829240-73829480 | Common:4; Rare:62 |