| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73612900-73613270 | Common:2; Rare:95 | ||||
| chr14:73633351-73634364 | Common:16; Rare:290 | ||||
| chr14:73663770-73664170 | Common:3; Rare:64 | ||||
| chr14:73696431-73697261 | Common:3; Rare:173; Clinvar:7; Clinvar (benign):1 | ||||
| chr14:73712208-73712973 | Common:4; Rare:490 | ||||
| chr14:73713186-73713586 | Common:2; Rare:154 | ||||
| chr14:73741430-73742310 | Common:11; Rare:229 | ||||
| chr14:73752779-73753193 | Common:2; Rare:122 | ||||
| chr14:73753310-73753710 | Rare:150 | ||||
| chr14:73754051-73754449 | Rare:166 | ||||
| chr14:73756342-73756586 | Rare:74 | ||||
| chr14:73757414-73757654 | Common:1; Rare:37 | ||||
| chr14:73757729-73758168 | Common:4; Rare:109 | ||||
| chr14:73758393-73758915 | Common:4; Rare:202 | ||||
| chr14:73761483-73761883 | Common:2; Rare:123 |