| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333924-103334258 | Common:3; Rare:143 | ||||
| chr14:103335916-103336116 | Rare:77 | ||||
| chr14:103519878-103520314 | Common:1; Rare:135 | ||||
| chr14:103521061-103521528 | Common:2; Rare:155; Clinvar:1 | ||||
| chr14:103529057-103529243 | Common:1; Rare:55 | ||||
| chr14:103562227-103562337 | Rare:49 | ||||
| chr14:103562619-103563078 | Common:8; Rare:181; Clinvar (benign):5 | ||||
| chr14:103629074-103629443 | Common:3; Rare:149 | ||||
| chr14:103715437-103715895 | Common:1; Rare:151 | ||||
| chr14:104773258-104773493 | Rare:55; Clinvar:4; Clinvar (benign):5 | ||||
| chr14:104970463-104970798 | Common:4; Rare:64 | ||||
| chr14:104985612-104985805 | Common:4; Rare:74 | ||||
| chr14:105301007-105301122 | Rare:21 | ||||
| chr14:105419737-105420027 | Rare:87 | ||||
| chr14:105487104-105487245 | Common:1; Rare:48 |