| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103561773-103562656 | Common:9; Rare:689 | ||||
| chr14:103562568-103563238 | Common:53; Rare:1252; Clinvar:2; Clinvar (benign):29 | ||||
| chr14:103628770-103629393 | Common:17; Rare:746 | ||||
| chr14:103629793-103630193 | Rare:108 | ||||
| chr14:103715297-103715866 | Common:7; Rare:1058 | ||||
| chr14:103847480-103847951 | Common:19; Rare:584 | ||||
| chr14:103921422-103921832 | Common:17; Rare:364 | ||||
| chr14:104689280-104689690 | Common:3; Rare:254; Clinvar (benign):1 | ||||
| chr14:104723947-104724960 | Common:18; Rare:686; Clinvar:2 | ||||
| chr14:104729320-104730224 | Common:42; Rare:791 | ||||
| chr14:104752542-104752820 | Common:7; Rare:265 | ||||
| chr14:104752859-104753259 | Common:12; Rare:528 | ||||
| chr14:104794537-104794937 | Common:2; Rare:81 | ||||
| chr14:104795483-104795926 | Rare:349 | ||||
| chr14:104800259-104800750 | Common:10; Rare:503 |