| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21437578-21437818 | Common:5; Rare:102 | ||||
| chr12:21501498-21501915 | Common:6; Rare:118 | ||||
| chr12:21657749-21658006 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774777-21775040 | Rare:51 | ||||
| chr12:22046123-22046360 | Common:1; Rare:79 | ||||
| chr12:22334611-22335067 | Common:1; Rare:128 | ||||
| chr12:22335972-22336079 | Rare:15 | ||||
| chr12:22544142-22544321 | Common:1; Rare:91 | ||||
| chr12:22544475-22544668 | Common:2; Rare:43 | ||||
| chr12:22625013-22625257 | Common:1; Rare:123 | ||||
| chr12:23949612-23949874 | Common:4; Rare:48 | ||||
| chr12:23950886-23951126 | Common:1; Rare:58 | ||||
| chr12:24948948-24949220 | Common:1; Rare:63 | ||||
| chr12:24949321-24949403 | Rare:19 | ||||
| chr12:25195142-25195340 | Common:1; Rare:56 |