| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:100535232-100535632 | Rare:109 | ||||
| chr5:103120072-103120461 | Common:1; Rare:100 | ||||
| chr5:103562732-103563020 | Common:7; Rare:97 | ||||
| chr5:108748679-108748991 | Common:2; Rare:107 | ||||
| chr5:109409314-109409487 | Common:1; Rare:55 | ||||
| chr5:109409849-109410295 | Common:4; Rare:168 | ||||
| chr5:110738923-110739078 | Common:2; Rare:60 | ||||
| chr5:111092247-111092410 | Common:2; Rare:88; Clinvar (benign):4 | ||||
| chr5:111512431-111512750 | Common:3; Rare:112 | ||||
| chr5:112707384-112707620 | Common:6; Rare:105; Clinvar:58; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr5:112861129-112861373 | Common:4; Rare:94 | ||||
| chr5:112976494-112976882 | Common:2; Rare:184 | ||||
| chr5:113294625-113294728 | Rare:25 | ||||
| chr5:113513635-113513725 | Rare:27 | ||||
| chr5:115262829-115262906 | Rare:39 |