| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:1592491-1592654 | Rare:36 | ||||
| chr12:1594579-1594897 | Common:1; Rare:95 | ||||
| chr12:2004382-2004664 | Common:1; Rare:101 | ||||
| chr12:2794944-2795234 | Rare:113 | ||||
| chr12:2798801-2799157 | Rare:87 | ||||
| chr12:2812487-2812731 | Common:1; Rare:62 | ||||
| chr12:2812891-2812988 | Rare:31 | ||||
| chr12:2876976-2877272 | Rare:93 | ||||
| chr12:2890702-2890953 | Common:1; Rare:101 | ||||
| chr12:2959802-2959944 | Common:1; Rare:39 | ||||
| chr12:3077233-3077451 | Common:7; Rare:93 | ||||
| chr12:4320942-4321279 | Common:5; Rare:131 | ||||
| chr12:4538431-4538942 | Common:3; Rare:117 | ||||
| chr12:4649049-4649178 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chr12:5431498-5431667 | Rare:41 |