| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6201242-6201388 | Common:2; Rare:34 | ||||
| chr12:6312716-6312749 | Rare:2 | ||||
| chr12:6333768-6333924 | Common:1; Rare:29; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:6341402-6341515 | Common:2; Rare:29 | ||||
| chr12:6341963-6342125 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6363352-6363497 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6363780-6363951 | Common:2; Rare:54 | ||||
| chr12:6363974-6364067 | Rare:27 | ||||
| chr12:6364097-6364130 | Rare:5 | ||||
| chr12:6364169-6364239 | Rare:17 | ||||
| chr12:6375200-6375744 | Common:5; Rare:129; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376110-6376538 | Common:4; Rare:87 | ||||
| chr12:6376730-6376882 | Rare:29 | ||||
| chr12:6377681-6377850 | Common:2; Rare:36 | ||||
| chr12:6377897-6377944 | Rare:8 |