| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32485837-32485981 | Rare:30 | ||||
| chr12:32534291-32534330 | Rare:12 | ||||
| chr12:32679037-32679364 | Common:2; Rare:128; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32679414-32679608 | Common:1; Rare:49 | ||||
| chr12:32679613-32679985 | Common:4; Rare:85 | ||||
| chr12:32755007-32755582 | Common:1; Rare:189; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr12:32755798-32756094 | Common:1; Rare:101 | ||||
| chr12:32756330-32756493 | Rare:35 | ||||
| chr12:32896351-32896930 | Common:6; Rare:175; Clinvar:20; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr12:32896949-32897313 | Common:3; Rare:105 | ||||
| chr12:34022325-34022541 | Common:2; Rare:58 | ||||
| chr12:38316945-38317079 | Common:1; Rare:54 | ||||
| chr12:38904863-38905258 | Rare:75 | ||||
| chr12:38905284-38905349 | Rare:18 | ||||
| chr12:38905486-38905798 | Common:5; Rare:88 |