| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132144326-132144486 | Rare:64 | ||||
| chr12:132687334-132687713 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132734502-132734686 | Rare:47 | ||||
| chr12:132887553-132887845 | Rare:85 | ||||
| chr12:132956276-132956435 | Common:1; Rare:32 | ||||
| chr12:133130238-133130652 | Common:7; Rare:137 | ||||
| chr13:19633454-19633751 | Common:1; Rare:114 | ||||
| chr13:19863538-19863954 | Common:6; Rare:156 | ||||
| chr13:20773940-20773967 | Rare:4 | ||||
| chr13:21061517-21061722 | Common:1; Rare:63 | ||||
| chr13:21140349-21140651 | Rare:130 | ||||
| chr13:21176545-21176713 | Common:1; Rare:84 | ||||
| chr13:21459177-21459519 | Common:1; Rare:122 | ||||
| chr13:23889332-23889567 | Common:1; Rare:82 | ||||
| chr13:24160509-24160780 | Rare:76 |