| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53973079-53973215 | Rare:66 | ||||
| chr12:53984729-53985480 | Common:10; Rare:368 | ||||
| chr12:53986309-53986654 | Common:2; Rare:66 | ||||
| chr12:53986555-53986655 | Rare:24 | ||||
| chr12:53994501-53994897 | Common:12; Rare:220 | ||||
| chr12:53995457-53995718 | Rare:110 | ||||
| chr12:53999810-54000380 | Common:10; Rare:310 | ||||
| chr12:54016729-54016920 | Rare:71 | ||||
| chr12:54188905-54189181 | Rare:120 | ||||
| chr12:54259060-54259440 | Rare:105 | ||||
| chr12:54259484-54259665 | Rare:60 | ||||
| chr12:54279661-54279878 | Rare:131 | ||||
| chr12:54280019-54280258 | Rare:151 | ||||
| chr12:54280511-54280810 | Common:2; Rare:151 | ||||
| chr12:54282941-54284012 | Common:9; Rare:495; Clinvar:5; Clinvar (pathogenic):6 |