| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56081860-56082250 | Rare:69 | ||||
| chr12:56129262-56129533 | Common:1; Rare:60 | ||||
| chr12:56634985-56635164 | Rare:55 | ||||
| chr12:57127141-57127480 | Rare:104 | ||||
| chr12:57138280-57138790 | Common:5; Rare:163 | ||||
| chr12:57148741-57149156 | Common:2; Rare:162 | ||||
| chr12:57239120-57239410 | Common:1; Rare:62 | ||||
| chr12:57545990-57546280 | Rare:119 | ||||
| chr12:57576189-57576297 | Rare:22 | ||||
| chr12:57576228-57576512 | Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:57579700-57580050 | Rare:125 | ||||
| chr12:57580030-57580530 | Common:2; Rare:103 | ||||
| chr12:57717890-57718570 | Common:4; Rare:290; Clinvar:2 | ||||
| chr12:57935980-57936360 | Common:7; Rare:130 | ||||
| chr12:62602724-62602858 | Rare:59 |