| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89709258-89709391 | Common:3; Rare:63 | ||||
| chr12:92929076-92929116 | Rare:13 | ||||
| chr12:92929218-92929521 | Common:1; Rare:94 | ||||
| chr12:93377728-93377970 | Rare:80 | ||||
| chr12:93441859-93442154 | Common:2; Rare:91 | ||||
| chr12:93571746-93571912 | Common:7; Rare:65 | ||||
| chr12:94459815-94460044 | Common:3; Rare:63 | ||||
| chr12:95217384-95217780 | Common:4; Rare:111 | ||||
| chr12:95858830-95859075 | Common:3; Rare:73 | ||||
| chr12:98515455-98515693 | Rare:75; Clinvar:1 | ||||
| chr12:98644850-98645300 | Common:4; Rare:125 | ||||
| chr12:100267065-100267316 | Common:1; Rare:107 | ||||
| chr12:101407663-101408076 | Common:3; Rare:103 | ||||
| chr12:101568106-101568364 | Common:2; Rare:49 | ||||
| chr12:101626863-101627018 | Rare:32; Clinvar:1; Clinvar (benign):1 |