| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31025223-31025878 | Common:16; Rare:661; Clinvar (benign):1 | ||||
| chr14:31026181-31026797 | Common:21; Rare:551 | ||||
| chr14:31026820-31027371 | Common:13; Rare:512 | ||||
| chr14:31105455-31105855 | Rare:96 | ||||
| chr14:31205744-31205903 | Rare:35 | ||||
| chr14:31205881-31207534 | Common:6; Rare:726 | ||||
| chr14:31207458-31207589 | Rare:37 | ||||
| chr14:31207604-31208127 | Common:13; Rare:788 | ||||
| chr14:31208050-31208844 | Common:14; Rare:472 | ||||
| chr14:31419705-31420228 | Common:7; Rare:216 | ||||
| chr14:31420427-31420884 | Common:27; Rare:626 | ||||
| chr14:31456610-31457080 | Common:2; Rare:82 | ||||
| chr14:31457330-31457710 | Common:8; Rare:321 | ||||
| chr14:31561060-31561680 | Common:18; Rare:577; Clinvar:15; Clinvar (benign):20; Clinvar (pathogenic):6 | ||||
| chr14:32076113-32077116 | Common:21; Rare:1293 |