| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:39443107-39443623 | Common:7; Rare:408; Clinvar:27; Clinvar (benign):16 | ||||
| chr12:39619665-39620210 | Common:9; Rare:350 | ||||
| chr12:39625927-39626327 | Common:3; Rare:189 | ||||
| chr12:39626468-39626868 | Common:1; Rare:103 | ||||
| chr12:40105406-40105806 | Common:4; Rare:145 | ||||
| chr12:40105960-40106310 | Common:3; Rare:307 | ||||
| chr12:40224601-40225136 | Common:15; Rare:272; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:42144670-42145524 | Common:37; Rare:778 | ||||
| chr12:42237483-42237691 | Rare:105 | ||||
| chr12:42237695-42237944 | Common:2; Rare:70 | ||||
| chr12:42238176-42238499 | Common:6; Rare:380 | ||||
| chr12:42325764-42326251 | Common:10; Rare:524 | ||||
| chr12:42442161-42442648 | Common:4; Rare:173 | ||||
| chr12:42442894-42443294 | Common:3; Rare:161 | ||||
| chr12:42482680-42483130 | Common:10; Rare:218 |