| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133080724-133080950 | Rare:71 | ||||
| chr12:133130225-133130996 | Common:8; Rare:228 | ||||
| chr12:133181364-133181596 | Common:2; Rare:71 | ||||
| chr12:133235821-133235900 | Common:1; Rare:28 | ||||
| chr13:19181700-19182087 | Common:12; Rare:157 | ||||
| chr13:19633518-19633814 | Common:3; Rare:114 | ||||
| chr13:19646235-19646523 | Rare:64 | ||||
| chr13:19782912-19783088 | Common:2; Rare:64 | ||||
| chr13:19863296-19863361 | Common:1; Rare:20 | ||||
| chr13:19863426-19863870 | Common:5; Rare:152 | ||||
| chr13:19958610-19958949 | Common:5; Rare:143 | ||||
| chr13:19958986-19959115 | Common:2; Rare:50 | ||||
| chr13:20161001-20161113 | Rare:46; Clinvar (benign):1 | ||||
| chr13:20525790-20525968 | Common:1; Rare:70 | ||||
| chr13:20567092-20567266 | Common:1; Rare:60 |