| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56909710-56910187 | Common:18; Rare:612 | ||||
| chr5:56910444-56910560 | Rare:38 | ||||
| chr5:56910575-56910975 | Common:3; Rare:62 | ||||
| chr5:56951391-56951791 | Common:5; Rare:100 | ||||
| chr5:56952020-56952685 | Common:2; Rare:474 | ||||
| chr5:57173220-57174150 | Common:14; Rare:1276 | ||||
| chr5:57174214-57174979 | Common:4; Rare:306 | ||||
| chr5:57175564-57175964 | Common:2; Rare:100 | ||||
| chr5:60699710-60699892 | Common:1; Rare:74 | ||||
| chr5:60699830-60700318 | Common:29; Rare:730 | ||||
| chr5:60700486-60700886 | Rare:78 | ||||
| chr5:60844128-60844528 | Common:28; Rare:590 | ||||
| chr5:60944906-60945380 | Common:35; Rare:742; Clinvar:31; Clinvar (benign):37; Clinvar (pathogenic):4 | ||||
| chr5:60945431-60945710 | Common:3; Rare:120 | ||||
| chr5:60945764-60946164 | Common:4; Rare:82 |