| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95961762-95962012 | Common:1; Rare:61 | ||||
| chr5:96702571-96702895 | Common:1; Rare:79 | ||||
| chr5:96876461-96876512 | Rare:9 | ||||
| chr5:96935848-96936144 | Common:8; Rare:99 | ||||
| chr5:97183178-97183581 | Common:4; Rare:152 | ||||
| chr5:98769893-98769940 | Rare:11 | ||||
| chr5:98773369-98773675 | Common:4; Rare:84 | ||||
| chr5:98928909-98929188 | Common:4; Rare:120 | ||||
| chr5:100535224-100535412 | Rare:45 | ||||
| chr5:103120082-103120440 | Common:1; Rare:90 | ||||
| chr5:108748665-108748993 | Common:2; Rare:117 | ||||
| chr5:109409852-109410017 | Common:4; Rare:74 | ||||
| chr5:110738863-110739072 | Common:2; Rare:68 | ||||
| chr5:111512445-111512872 | Common:4; Rare:141 | ||||
| chr5:112737743-112737911 | Rare:37; Clinvar:1; Clinvar (benign):2 |