| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73713658-73714063 | Common:1; Rare:111 | ||||
| chr14:73714353-73714469 | Common:1; Rare:44 | ||||
| chr14:73787129-73787379 | Common:2; Rare:88 | ||||
| chr14:73851733-73851983 | Common:4; Rare:85 | ||||
| chr14:73950262-73950521 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:74019201-74019496 | Common:2; Rare:110 | ||||
| chr14:74084375-74085003 | Common:9; Rare:189 | ||||
| chr14:74302915-74303079 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr14:74493240-74493813 | Common:4; Rare:191; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74494166-74494364 | Rare:63; Clinvar (benign):1 | ||||
| chr14:74713042-74713213 | Rare:96 | ||||
| chr14:74763231-74763452 | Rare:75 | ||||
| chr14:74809691-74809923 | Rare:65 | ||||
| chr14:74881778-74882207 | Common:1; Rare:173 | ||||
| chr14:74955590-74955761 | Common:1; Rare:37 |