| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355540-126355742 | Common:1; Rare:49 | ||||
| chr11:134253306-134253576 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr12:2877039-2877234 | Rare:51 | ||||
| chr12:6493240-6493502 | Common:6; Rare:78 | ||||
| chr12:6493789-6494126 | Common:2; Rare:101 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6970630-6970952 | Common:3; Rare:101 | ||||
| chr12:10613540-10613671 | Common:1; Rare:54 | ||||
| chr12:11171604-11171705 | Common:1; Rare:34 | ||||
| chr12:14803458-14803693 | Common:1; Rare:62 | ||||
| chr12:15882307-15882411 | Rare:37 | ||||
| chr12:21501564-21501828 | Common:1; Rare:63 | ||||
| chr12:26938282-26938526 | Common:3; Rare:92 | ||||
| chr12:27523990-27524158 | Rare:42 | ||||
| chr12:42326065-42326167 | Common:1; Rare:32 |