| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972575-123972895 | Common:6; Rare:113 | ||||
| chr12:130871730-130872104 | Common:4; Rare:157 | ||||
| chr12:131710835-131711131 | Common:1; Rare:75 | ||||
| chr12:131929035-131929284 | Common:10; Rare:76; Clinvar:1 | ||||
| chr12:131949624-131949975 | Common:2; Rare:110 | ||||
| chr12:132687311-132687689 | Common:4; Rare:141; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887548-132887844 | Rare:87 | ||||
| chr12:132956280-132956383 | Common:1; Rare:22 | ||||
| chr12:132986210-132986428 | Rare:50 | ||||
| chr12:133130230-133130652 | Common:7; Rare:140 | ||||
| chr12:133181378-133181550 | Common:1; Rare:51 | ||||
| chr13:19633359-19633737 | Common:1; Rare:140 | ||||
| chr13:19863538-19863870 | Common:5; Rare:122 | ||||
| chr13:21176545-21176711 | Common:1; Rare:83 |