| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77800250-77800710 | Common:2; Rare:88 | ||||
| chr14:79279050-79279540 | Common:3; Rare:114 | ||||
| chr14:80941694-80942011 | Common:5; Rare:77 | ||||
| chr14:81220861-81221225 | Common:1; Rare:150 | ||||
| chr14:81221275-81221572 | Common:1; Rare:92 | ||||
| chr14:81323955-81324501 | Common:5; Rare:235 | ||||
| chr14:81436451-81436604 | Rare:56 | ||||
| chr14:81533794-81534215 | Rare:116 | ||||
| chr14:85529064-85530312 | Common:12; Rare:305 | ||||
| chr14:87993096-87993345 | Common:4; Rare:107; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:88323210-88323760 | Common:2; Rare:157 | ||||
| chr14:88385497-88385819 | Common:2; Rare:105; Clinvar:3 | ||||
| chr14:88551290-88551690 | Common:3; Rare:121 | ||||
| chr14:88554745-88554951 | Common:2; Rare:56 | ||||
| chr14:88562907-88563101 | Rare:93 |