| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24259411-24259532 | Rare:31 | ||||
| chr14:32203265-32203661 | Common:13; Rare:169 | ||||
| chr14:34874125-34874232 | Common:1; Rare:30 | ||||
| chr14:35401997-35402135 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:36647165-36647375 | Common:4; Rare:54 | ||||
| chr14:36655958-36656223 | Common:2; Rare:49 | ||||
| chr14:36658746-36659029 | Common:2; Rare:61 | ||||
| chr14:36659950-36660105 | Common:2; Rare:38 | ||||
| chr14:49633903-49634047 | Common:1; Rare:61; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr14:49862630-49863048 | Common:1; Rare:188 | ||||
| chr14:49868106-49868343 | Common:1; Rare:47 | ||||
| chr14:50001286-50001497 | Common:3; Rare:51 | ||||
| chr14:50009062-50009213 | Rare:27 | ||||
| chr14:50039800-50039994 | Common:2; Rare:44 | ||||
| chr14:50040554-50040681 | Rare:14 |