| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188488-49188583 | Common:1; Rare:14 | ||||
| chr12:49188959-49189394 | Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49292793-49292961 | Rare:33 | ||||
| chr12:49293091-49293722 | Common:2; Rare:118 | ||||
| chr12:49294939-49295173 | Common:3; Rare:47 | ||||
| chr12:49295350-49295450 | Rare:38 | ||||
| chr12:49322964-49323344 | Common:5; Rare:93 | ||||
| chr12:49337105-49337340 | Common:2; Rare:49 | ||||
| chr12:49366800-49367021 | Rare:54 | ||||
| chr12:49367131-49367581 | Common:2; Rare:124 | ||||
| chr12:49568072-49568443 | Common:2; Rare:90 | ||||
| chr12:49623313-49623574 | Common:1; Rare:67 | ||||
| chr12:49741258-49741607 | Rare:99 | ||||
| chr12:49828398-49828600 | Rare:73 | ||||
| chr12:49843057-49843179 | Common:1; Rare:54; Clinvar (benign):1 |