| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14802988-14803205 | Common:2; Rare:55 | ||||
| chr12:14803354-14803731 | Common:3; Rare:105 | ||||
| chr12:14803994-14804281 | Common:2; Rare:47 | ||||
| chr12:14884217-14884512 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:14885760-14885833 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr12:14885836-14886091 | Common:6; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:15348661-15349005 | Common:4; Rare:83 | ||||
| chr12:15882232-15882816 | Common:1; Rare:196 | ||||
| chr12:15911204-15911400 | Common:5; Rare:76 | ||||
| chr12:18714771-18714805 | Common:2; Rare:9 | ||||
| chr12:18737933-18738398 | Common:4; Rare:114 | ||||
| chr12:19129402-19129814 | Common:3; Rare:169 | ||||
| chr12:19439312-19439727 | Common:3; Rare:154 | ||||
| chr12:19440170-19440377 | Rare:62 | ||||
| chr12:19440563-19440664 | Common:1; Rare:35 |