| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12717570-12717643 | Rare:24; Clinvar (benign):3 | ||||
| chr12:12718236-12718336 | Rare:49; Clinvar:6; Clinvar (benign):6 | ||||
| chr12:12725012-12725552 | Common:4; Rare:136 | ||||
| chr12:12725554-12725616 | Common:1; Rare:11 | ||||
| chr12:12725622-12725735 | Common:1; Rare:29 | ||||
| chr12:12725764-12725993 | Common:2; Rare:45 | ||||
| chr12:12726062-12726162 | Common:1; Rare:19 | ||||
| chr12:12813235-12813452 | Common:1; Rare:63 | ||||
| chr12:12890594-12890805 | Common:1; Rare:36 | ||||
| chr12:12890807-12891074 | Rare:54 | ||||
| chr12:12891112-12891720 | Common:3; Rare:116 | ||||
| chr12:12999804-12999914 | Rare:22 | ||||
| chr12:13000008-13000049 | Rare:12 | ||||
| chr12:13000207-13000588 | Common:2; Rare:102 | ||||
| chr12:13044284-13044433 | Rare:38 |