| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98644711-98644843 | Common:3; Rare:45 | ||||
| chr12:98644986-98645317 | Common:2; Rare:98 | ||||
| chr12:100200707-100200826 | Rare:35 | ||||
| chr12:100267047-100267403 | Common:1; Rare:149 | ||||
| chr12:100573551-100573830 | Rare:90 | ||||
| chr12:101209862-101209947 | Common:2; Rare:29 | ||||
| chr12:101210236-101210267 | Rare:8 | ||||
| chr12:101407697-101408049 | Common:3; Rare:82 | ||||
| chr12:101697459-101697685 | Common:2; Rare:67 | ||||
| chr12:101790067-101790105 | Common:1; Rare:11; Clinvar (benign):2 | ||||
| chr12:101877275-101877346 | Common:1; Rare:13 | ||||
| chr12:101877500-101877927 | Common:5; Rare:123 | ||||
| chr12:102061251-102061523 | Rare:61 | ||||
| chr12:102120061-102120251 | Rare:73 | ||||
| chr12:103930007-103930571 | Common:9; Rare:183 |