| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515455-98515657 | Rare:66; Clinvar:1 | ||||
| chr12:98593456-98593776 | Common:2; Rare:106; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644986-98645296 | Common:2; Rare:92 | ||||
| chr12:100573554-100573740 | Rare:65 | ||||
| chr12:101407654-101408035 | Common:3; Rare:95 | ||||
| chr12:102120065-102120224 | Rare:60 | ||||
| chr12:102478536-102478645 | Rare:23 | ||||
| chr12:103930030-103930520 | Common:9; Rare:162 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064322-104064555 | Common:1; Rare:58 | ||||
| chr12:104138152-104138415 | Common:1; Rare:74 | ||||
| chr12:105107619-105107789 | Common:1; Rare:78 | ||||
| chr12:105236124-105236307 | Common:1; Rare:83 | ||||
| chr12:106357470-106357823 | Common:4; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106987049-106987286 | Common:4; Rare:67 |