| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22770578-22770863 | Common:2; Rare:64 | ||||
| chr14:23381764-23382076 | Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23385918-23386661 | Common:10; Rare:256; Clinvar:35; Clinvar (benign):24 | ||||
| chr14:23387522-23387930 | Common:2; Rare:151; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr14:23389377-23389723 | Rare:113; Clinvar:17; Clinvar (benign):13 | ||||
| chr14:23393323-23393913 | Common:3; Rare:150; Clinvar:14; Clinvar (benign):9 | ||||
| chr14:23396668-23397084 | Common:4; Rare:130; Clinvar:11; Clinvar (benign):10 | ||||
| chr14:23399371-23399652 | Common:4; Rare:59 | ||||
| chr14:23402445-23402915 | Common:4; Rare:147; Clinvar:11; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr14:23405084-23405381 | Common:5; Rare:84; Clinvar:6; Clinvar (benign):7 | ||||
| chr14:23409560-23409827 | Common:2; Rare:50 | ||||
| chr14:23410037-23410329 | Common:2; Rare:61 | ||||
| chr14:23414392-23414598 | Common:2; Rare:42 | ||||
| chr14:23415379-23416320 | Common:2; Rare:290; Clinvar:51; Clinvar (benign):32; Clinvar (pathogenic):10 | ||||
| chr14:23416866-23417320 | Common:4; Rare:131; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):6 |