| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95961811-95961861 | Rare:10 | ||||
| chr5:96702564-96702876 | Common:1; Rare:78 | ||||
| chr5:96935824-96936119 | Common:10; Rare:99 | ||||
| chr5:97183203-97183521 | Common:4; Rare:117 | ||||
| chr5:98928921-98929188 | Common:3; Rare:117 | ||||
| chr5:100535235-100535413 | Rare:43 | ||||
| chr5:100903207-100903391 | Common:1; Rare:33 | ||||
| chr5:103120086-103120410 | Common:1; Rare:78 | ||||
| chr5:108382052-108382141 | Common:1; Rare:34 | ||||
| chr5:108748688-108748985 | Common:2; Rare:100 | ||||
| chr5:109409847-109410136 | Common:4; Rare:108 | ||||
| chr5:110738936-110739078 | Common:2; Rare:56 | ||||
| chr5:111757152-111757254 | Common:4; Rare:19 | ||||
| chr5:112737722-112737923 | Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:112976477-112976840 | Common:2; Rare:163 |