| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58199785-58200265 | Common:7; Rare:324 | ||||
| chr14:58244618-58245030 | Rare:237 | ||||
| chr14:58244970-58245750 | Common:4; Rare:221 | ||||
| chr14:58263304-58263774 | Common:2; Rare:228 | ||||
| chr14:58297732-58297970 | Common:3; Rare:180 | ||||
| chr14:58298016-58298670 | Common:1; Rare:505 | ||||
| chr14:58298975-58299417 | Common:12; Rare:269 | ||||
| chr14:58299388-58299912 | Common:3; Rare:241 | ||||
| chr14:58395830-58396127 | Rare:193 | ||||
| chr14:58396343-58396513 | Rare:88 | ||||
| chr14:58427019-58427429 | Common:7; Rare:229 | ||||
| chr14:58427474-58427816 | Rare:256 | ||||
| chr14:58428385-58428565 | Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:59188343-59189082 | Common:8; Rare:441 | ||||
| chr14:59263023-59263701 | Rare:252 |