| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95731019-95731330 | Rare:104 | ||||
| chr5:95961773-95962012 | Common:1; Rare:59 | ||||
| chr5:97183266-97183579 | Common:2; Rare:106 | ||||
| chr5:100535235-100535422 | Rare:44 | ||||
| chr5:108748688-108748976 | Common:2; Rare:95 | ||||
| chr5:109409283-109409585 | Common:4; Rare:98 | ||||
| chr5:111757164-111757470 | Common:6; Rare:73 | ||||
| chr5:115602099-115602230 | Common:2; Rare:45 | ||||
| chr5:115841833-115841963 | Common:1; Rare:45 | ||||
| chr5:119452567-119452750 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:122077092-122077303 | Common:1; Rare:37 | ||||
| chr5:122077822-122078409 | Rare:157; Clinvar:1 | ||||
| chr5:126423347-126423571 | Rare:59 | ||||
| chr5:132556889-132556988 | Rare:38; Clinvar:1 | ||||
| chr5:132866467-132866674 | Common:1; Rare:64 |