| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57549711-57550111 | Common:1; Rare:276 | ||||
| chr12:57590458-57591466 | Common:34; Rare:828 | ||||
| chr12:57611147-57611547 | Common:1; Rare:189 | ||||
| chr12:57611575-57612187 | Common:9; Rare:316 | ||||
| chr12:57614320-57614437 | Rare:57 | ||||
| chr12:57632071-57632605 | Common:8; Rare:235 | ||||
| chr12:57632512-57632920 | Common:3; Rare:188 | ||||
| chr12:57633015-57633415 | Common:1; Rare:184 | ||||
| chr12:57693757-57694253 | Common:3; Rare:335 | ||||
| chr12:57694413-57694813 | Rare:88 | ||||
| chr12:57744428-57744828 | Rare:118 | ||||
| chr12:57744789-57745117 | Common:1; Rare:258 | ||||
| chr12:57745038-57745390 | Common:5; Rare:153 | ||||
| chr12:57745753-57746153 | Common:2; Rare:119 | ||||
| chr12:57750745-57751819 | Common:8; Rare:643; Clinvar:103; Clinvar (benign):77; Clinvar (pathogenic):2 |