| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113841929-113842103 | Common:20; Rare:41 | ||||
| chr14:20799945-20800093 | Common:13; Rare:19 | ||||
| chr14:22770804-22771041 | Rare:67 | ||||
| chr14:23387527-23387925 | Common:2; Rare:147; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr14:23389391-23389713 | Rare:107; Clinvar:17; Clinvar (benign):12 | ||||
| chr14:23393342-23393909 | Common:3; Rare:143; Clinvar:14; Clinvar (benign):9 | ||||
| chr14:23402599-23402926 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):4 | ||||
| chr14:23410059-23410311 | Common:2; Rare:53 | ||||
| chr14:23411757-23412079 | Common:2; Rare:45 | ||||
| chr14:23415326-23415853 | Common:1; Rare:166; Clinvar:23; Clinvar (benign):16; Clinvar (pathogenic):5 | ||||
| chr14:23416373-23416616 | Common:3; Rare:43 | ||||
| chr14:23416836-23417069 | Common:3; Rare:72; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr14:23418054-23418425 | Common:1; Rare:103; Clinvar:19; Clinvar (benign):11; Clinvar (pathogenic):4 | ||||
| chr14:23420720-23420896 | Rare:27 | ||||
| chr14:23423540-23424194 | Common:3; Rare:175; Clinvar:21; Clinvar (benign):20; Clinvar (pathogenic):10 |