| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:98928873-98929196 | Common:4; Rare:133 | ||||
| chr5:100535215-100535774 | Common:1; Rare:166 | ||||
| chr5:100903213-100903408 | Rare:39 | ||||
| chr5:103120106-103120430 | Common:1; Rare:80 | ||||
| chr5:108748679-108748993 | Common:2; Rare:109 | ||||
| chr5:109409841-109410053 | Common:4; Rare:87 | ||||
| chr5:110738906-110739192 | Common:2; Rare:113; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:110752994-110753160 | Common:1; Rare:29 | ||||
| chr5:112419096-112419309 | Common:3; Rare:78 | ||||
| chr5:112707492-112707791 | Common:4; Rare:119; Clinvar:57; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr5:112921204-112921348 | Common:1; Rare:65 | ||||
| chr5:112922128-112922435 | Common:2; Rare:122 | ||||
| chr5:113294560-113294760 | Rare:58 | ||||
| chr5:115262837-115262888 | Rare:25 | ||||
| chr5:115544738-115545014 | Common:2; Rare:110 |