| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515227-98515872 | Common:4; Rare:948; Clinvar:17; Clinvar (benign):2 | ||||
| chr12:98515995-98516101 | Rare:45; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:98516054-98517063 | Common:24; Rare:1034; Clinvar:6; Clinvar (benign):14 | ||||
| chr12:98592797-98593197 | Common:2; Rare:77 | ||||
| chr12:98593368-98593810 | Common:8; Rare:531; Clinvar:16; Clinvar (benign):16 | ||||
| chr12:98644267-98644667 | Rare:141 | ||||
| chr12:98644570-98645350 | Common:26; Rare:1033 | ||||
| chr12:99984370-99984810 | Common:2; Rare:123 | ||||
| chr12:99984830-99985229 | Common:3; Rare:96 | ||||
| chr12:100142715-100143115 | Common:11; Rare:422 | ||||
| chr12:100199028-100200980 | Common:21; Rare:898 | ||||
| chr12:100201073-100201226 | Common:1; Rare:26 | ||||
| chr12:100266320-100266905 | Common:4; Rare:355 | ||||
| chr12:100266955-100267688 | Common:16; Rare:1099 | ||||
| chr12:100573440-100573818 | Rare:537 |