| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14843458-14843683 | Common:2; Rare:82 | ||||
| chr12:14885721-14886063 | Common:10; Rare:98; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:14886080-14886816 | Common:14; Rare:258 | ||||
| chr12:14928950-14929410 | Common:5; Rare:148 | ||||
| chr12:14948790-14949090 | Common:2; Rare:69 | ||||
| chr12:14951129-14951262 | Common:1; Rare:25 | ||||
| chr12:14960990-14961380 | Common:6; Rare:80 | ||||
| chr12:15221190-15221800 | Common:5; Rare:350 | ||||
| chr12:15789257-15789664 | Common:2; Rare:335 | ||||
| chr12:15882053-15882542 | Common:3; Rare:315 | ||||
| chr12:15911176-15911413 | Common:15; Rare:204 | ||||
| chr12:15911431-15911831 | Rare:121 | ||||
| chr12:16347479-16347897 | Common:10; Rare:152 | ||||
| chr12:16347990-16348560 | Common:4; Rare:103 | ||||
| chr12:16350770-16351130 | Common:2; Rare:72 |