| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179820773-179820939 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179823969-179824238 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179858969 | Rare:96 | ||||
| chr5:179907776-179908009 | Common:2; Rare:109 | ||||
| chr5:180802766-180802928 | Common:4; Rare:70 | ||||
| chr5:180803821-180803948 | Common:1; Rare:28 | ||||
| chr5:180810102-180810223 | Common:1; Rare:26 | ||||
| chr5:180861150-180861394 | Common:2; Rare:98 | ||||
| chr5:181040121-181040335 | Rare:40 | ||||
| chr5:181223118-181223332 | Rare:76 | ||||
| chr5:181223645-181223755 | Common:3; Rare:27 | ||||
| chr5:181243690-181243875 | Common:2; Rare:58 | ||||
| chr5:181261049-181261271 | Rare:76 | ||||
| chr6:1311796-1312133 | Common:3; Rare:102 | ||||
| chr6:2245425-2245840 | Common:1; Rare:140 |