| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133130226-133130652 | Common:7; Rare:142 | ||||
| chr13:19633454-19633751 | Common:1; Rare:114 | ||||
| chr13:19863433-19863619 | Common:2; Rare:56 | ||||
| chr13:19863627-19863977 | Common:4; Rare:135 | ||||
| chr13:20525796-20525936 | Common:1; Rare:58 | ||||
| chr13:20567058-20567256 | Common:1; Rare:67 | ||||
| chr13:20773897-20774034 | Rare:51 | ||||
| chr13:21140374-21140678 | Rare:127 | ||||
| chr13:21176522-21176724 | Common:1; Rare:96 | ||||
| chr13:21603818-21603930 | Rare:47 | ||||
| chr13:21604100-21604285 | Common:4; Rare:100 | ||||
| chr13:21670946-21671160 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23579247-23579383 | Common:2; Rare:40 | ||||
| chr13:23889298-23889497 | Common:1; Rare:73 | ||||
| chr13:24160528-24160817 | Common:1; Rare:82 |