| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108382075-108382186 | Common:1; Rare:37 | ||||
| chr5:108747818-108747987 | Rare:22 | ||||
| chr5:108748679-108748992 | Common:2; Rare:108 | ||||
| chr5:109409814-109410018 | Common:4; Rare:81 | ||||
| chr5:109689135-109689458 | Common:5; Rare:135 | ||||
| chr5:109689827-109690011 | Common:2; Rare:67 | ||||
| chr5:110738906-110739137 | Common:2; Rare:95; Clinvar (pathogenic):1 | ||||
| chr5:111092181-111092434 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111512389-111512595 | Common:1; Rare:66 | ||||
| chr5:111757178-111757335 | Common:5; Rare:31 | ||||
| chr5:112419180-112419293 | Common:1; Rare:52 | ||||
| chr5:112976477-112976859 | Common:2; Rare:178 | ||||
| chr5:113203257-113203413 | Common:2; Rare:42 | ||||
| chr5:113294591-113294684 | Rare:32 | ||||
| chr5:115262813-115262927 | Common:1; Rare:55 |