| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:71321037-71321486 | Common:6; Rare:182 | ||||
| chr14:71321742-71321931 | Common:2; Rare:65 | ||||
| chr14:72894092-72894264 | Common:8; Rare:120 | ||||
| chr14:72926209-72926530 | Common:7; Rare:144 | ||||
| chr14:73026980-73027380 | Common:4; Rare:189 | ||||
| chr14:73058301-73058654 | Common:6; Rare:211 | ||||
| chr14:73136197-73136581 | Common:5; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73136610-73137300 | Common:2; Rare:178 | ||||
| chr14:73457750-73458332 | Common:17; Rare:198 | ||||
| chr14:73458397-73458872 | Common:10; Rare:223 | ||||
| chr14:73490850-73491009 | Common:4; Rare:60 | ||||
| chr14:73536834-73537180 | Common:10; Rare:41 | ||||
| chr14:73537787-73537956 | Common:4; Rare:37 | ||||
| chr14:73568750-73569040 | Common:1; Rare:44 | ||||
| chr14:73569029-73569292 | Rare:59 |