| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:96373070-96373334 | Common:1; Rare:47 | ||||
| chr5:96503608-96503663 | Common:1; Rare:13 | ||||
| chr5:96934164-96934422 | Common:1; Rare:45 | ||||
| chr5:98927276-98927386 | Common:1; Rare:22 | ||||
| chr5:102755976-102756195 | Common:2; Rare:35 | ||||
| chr5:111374449-111374723 | Common:3; Rare:50 | ||||
| chr5:112160808-112161144 | Common:3; Rare:139 | ||||
| chr5:112333412-112333646 | Common:2; Rare:42 | ||||
| chr5:112420382-112420536 | Common:3; Rare:42 | ||||
| chr5:112554386-112554392 | Rare:3 | ||||
| chr5:112628300-112628434 | Rare:26 | ||||
| chr5:112800987-112801325 | Common:1; Rare:87; Clinvar:10; Clinvar (benign):10 | ||||
| chr5:116573023-116573383 | Common:3; Rare:124 | ||||
| chr5:124651647-124651864 | Common:2; Rare:68 | ||||
| chr5:124749337-124749565 | Rare:50 |