| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501494-21501938 | Common:6; Rare:130 | ||||
| chr12:21527296-21527540 | Common:1; Rare:64 | ||||
| chr12:21527916-21527968 | Rare:12 | ||||
| chr12:21657733-21658006 | Common:4; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22250823-22251108 | Common:2; Rare:43 | ||||
| chr12:22334639-22335023 | Common:1; Rare:113 | ||||
| chr12:22477283-22477420 | Common:3; Rare:10 | ||||
| chr12:22544157-22544296 | Common:1; Rare:72 | ||||
| chr12:22544483-22544652 | Common:2; Rare:38 | ||||
| chr12:22624997-22625257 | Common:1; Rare:124 | ||||
| chr12:23949579-23949914 | Common:5; Rare:70 | ||||
| chr12:23950223-23950408 | Common:2; Rare:49 | ||||
| chr12:23950884-23951106 | Common:1; Rare:55 | ||||
| chr12:25195158-25195338 | Common:1; Rare:53 | ||||
| chr12:25959371-25959390 | Rare:2 |