| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178208120-178208252 | Common:1; Rare:32 | ||||
| chr5:178213874-178213966 | Rare:15 | ||||
| chr5:178218654-178218861 | Rare:36 | ||||
| chr5:178226651-178226757 | Rare:22 | ||||
| chr5:179798021-179798177 | Common:1; Rare:55 | ||||
| chr5:179832974-179833064 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:180830868-180831035 | Common:1; Rare:52 | ||||
| chr5:180831567-180831679 | Common:2; Rare:47 | ||||
| chr5:181191825-181192054 | Common:2; Rare:76 | ||||
| chr5:181207564-181207751 | Common:4; Rare:58 | ||||
| chr5:181246409-181246538 | Common:3; Rare:47 | ||||
| chr6:711403-711491 | Rare:12 | ||||
| chr6:2272628-2272842 | Common:2; Rare:29 | ||||
| chr6:3285443-3285446 | |||||
| chr6:3298509-3298531 | Rare:8 |