| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:103120072-103120393 | Common:1; Rare:77 | ||||
| chr5:103258669-103258810 | Common:1; Rare:56 | ||||
| chr5:108748665-108748993 | Common:2; Rare:117 | ||||
| chr5:109408912-109409115 | Common:4; Rare:52 | ||||
| chr5:109409841-109410297 | Common:4; Rare:169 | ||||
| chr5:109689236-109689434 | Common:4; Rare:92 | ||||
| chr5:110738906-110739147 | Common:2; Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:111092233-111092442 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111757146-111757255 | Common:4; Rare:21 | ||||
| chr5:111757318-111757345 | Rare:6 | ||||
| chr5:111757553-111757815 | Common:1; Rare:104 | ||||
| chr5:112419187-112419287 | Common:1; Rare:43 | ||||
| chr5:112976544-112976881 | Common:2; Rare:158 | ||||
| chr5:113294625-113294700 | Rare:20 | ||||
| chr5:113513624-113513705 | Rare:27 |