| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77457516-77457885 | Common:2; Rare:113 | ||||
| chr14:77707985-77708201 | Common:2; Rare:111 | ||||
| chr14:81220690-81221046 | Common:3; Rare:135 | ||||
| chr14:81221269-81221471 | Common:1; Rare:49 | ||||
| chr14:81436421-81436567 | Common:1; Rare:54 | ||||
| chr14:85529950-85530184 | Common:2; Rare:46 | ||||
| chr14:87989713-87989911 | Common:4; Rare:35 | ||||
| chr14:87993010-87993268 | Common:4; Rare:127; Clinvar:13; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr14:88562907-88563161 | Rare:113 | ||||
| chr14:88563464-88563572 | Rare:52 | ||||
| chr14:88824361-88824719 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89619045-89619260 | Common:1; Rare:76 | ||||
| chr14:89954644-89954950 | Rare:96 | ||||
| chr14:89955845-89955977 | Common:4; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331918-90332202 | Common:1; Rare:77 |