| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95473961-95474022 | Rare:19 | ||||
| chr12:95474030-95474203 | Common:2; Rare:83 | ||||
| chr12:95548800-95548914 | Common:2; Rare:42 | ||||
| chr12:96400556-96400710 | Rare:71 | ||||
| chr12:96907174-96907295 | Rare:44 | ||||
| chr12:98515313-98515873 | Common:1; Rare:203; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593467-98593770 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98645007-98645293 | Common:2; Rare:87 | ||||
| chr12:100142842-100143078 | Common:3; Rare:88 | ||||
| chr12:100267063-100267161 | Rare:43 | ||||
| chr12:100573599-100573716 | Rare:34 | ||||
| chr12:101280027-101280155 | Common:1; Rare:41 | ||||
| chr12:101407714-101408074 | Common:3; Rare:89 | ||||
| chr12:102120043-102120269 | Common:1; Rare:92 | ||||
| chr12:103441559-103441791 | Rare:37 |