| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526916-122527300 | Common:3; Rare:122 | ||||
| chr12:122980571-122980811 | Common:1; Rare:82 | ||||
| chr12:123233096-123233482 | Common:2; Rare:125; Clinvar:1 | ||||
| chr12:123364825-123364988 | Common:3; Rare:59 | ||||
| chr12:123584324-123584609 | Common:5; Rare:94 | ||||
| chr12:123601806-123602144 | Common:6; Rare:86 | ||||
| chr12:123633624-123633856 | Common:1; Rare:107; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:130871735-130872116 | Common:4; Rare:159 | ||||
| chr12:132687368-132687690 | Common:4; Rare:110 | ||||
| chr13:19633527-19633737 | Common:1; Rare:82 | ||||
| chr13:19782943-19783088 | Common:2; Rare:55 | ||||
| chr13:20525862-20525941 | Rare:36 | ||||
| chr13:21140401-21140615 | Rare:102 | ||||
| chr13:21176473-21176713 | Common:2; Rare:107 | ||||
| chr13:23889338-23889591 | Common:1; Rare:88 |