| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95548803-95548942 | Common:2; Rare:45 | ||||
| chr12:95996260-95996482 | Common:2; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96194240-96194626 | Common:5; Rare:123 | ||||
| chr12:96399371-96399468 | Common:1; Rare:28 | ||||
| chr12:96400527-96400680 | Common:1; Rare:70 | ||||
| chr12:96907174-96907293 | Rare:42 | ||||
| chr12:98515470-98515697 | Rare:71; Clinvar:1 | ||||
| chr12:98593462-98593771 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644731-98644843 | Common:1; Rare:36 | ||||
| chr12:98645067-98645305 | Common:2; Rare:64 | ||||
| chr12:100200553-100200854 | Common:3; Rare:89 | ||||
| chr12:100267063-100267299 | Common:1; Rare:105 | ||||
| chr12:100573554-100573770 | Rare:74 | ||||
| chr12:101407677-101408035 | Common:3; Rare:83 | ||||
| chr12:101877515-101877781 | Common:4; Rare:72 |