| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687322-132687706 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132710732-132711023 | Common:4; Rare:97 | ||||
| chr12:132887548-132887820 | Rare:81 | ||||
| chr12:132956271-132956370 | Common:1; Rare:25 | ||||
| chr12:132986264-132986428 | Rare:36 | ||||
| chr12:133080733-133080934 | Rare:63 | ||||
| chr12:133130232-133130652 | Common:7; Rare:139 | ||||
| chr13:19633472-19633746 | Common:1; Rare:107 | ||||
| chr13:19646329-19646583 | Rare:58 | ||||
| chr13:20525790-20525936 | Common:1; Rare:62 | ||||
| chr13:20567067-20567173 | Rare:35 | ||||
| chr13:21140257-21140630 | Rare:157 | ||||
| chr13:21176563-21176711 | Rare:78 | ||||
| chr13:23889345-23889556 | Common:1; Rare:73 | ||||
| chr13:24512729-24512834 | Common:1; Rare:32 |