| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76812763-76813019 | Common:3; Rare:203 | ||||
| chr14:77028375-77028516 | Common:5; Rare:58 | ||||
| chr14:77028551-77028952 | Rare:198 | ||||
| chr14:77097851-77098371 | Rare:323 | ||||
| chr14:77320774-77321152 | Common:2; Rare:194; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:77321160-77321540 | Common:10; Rare:286 | ||||
| chr14:77377038-77377411 | Common:5; Rare:213 | ||||
| chr14:77457486-77457844 | Common:2; Rare:201 | ||||
| chr14:77458007-77458235 | Rare:109 | ||||
| chr14:77616568-77617089 | Common:4; Rare:206; Clinvar:3; Clinvar (benign):5 | ||||
| chr14:77707988-77708197 | Common:2; Rare:160 | ||||
| chr14:77761101-77761262 | Rare:117 | ||||
| chr14:77800013-77800163 | Rare:49 | ||||
| chr14:77800194-77800594 | Common:8; Rare:144 | ||||
| chr14:81220684-81221122 | Common:4; Rare:281 |