| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:96935824-96936132 | Common:10; Rare:104 | ||||
| chr5:98928921-98929171 | Common:3; Rare:112 | ||||
| chr5:100535230-100535378 | Rare:35 | ||||
| chr5:100903149-100903418 | Common:1; Rare:51 | ||||
| chr5:100903639-100903840 | Common:2; Rare:29 | ||||
| chr5:103120086-103120398 | Common:1; Rare:74 | ||||
| chr5:108748757-108748976 | Common:1; Rare:73 | ||||
| chr5:110738929-110739057 | Common:1; Rare:45 | ||||
| chr5:111092261-111092388 | Common:2; Rare:74; Clinvar (benign):4 | ||||
| chr5:111512457-111512751 | Common:3; Rare:107 | ||||
| chr5:112976544-112976850 | Common:2; Rare:138 | ||||
| chr5:115262849-115262937 | Rare:42 | ||||
| chr5:115841544-115841619 | Common:1; Rare:45 | ||||
| chr5:115841809-115842081 | Common:4; Rare:85 | ||||
| chr5:116084937-116085055 | Common:4; Rare:52 |