| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31459048-31459188 | Rare:40 | ||||
| chr16:31459314-31459550 | Common:1; Rare:101 | ||||
| chr16:31459735-31460220 | Common:1; Rare:206 | ||||
| chr16:31471836-31472439 | Common:1; Rare:216 | ||||
| chr16:31507527-31508301 | Common:6; Rare:315 | ||||
| chr16:31508328-31508588 | Common:4; Rare:105 | ||||
| chr16:31713082-31713368 | Common:1; Rare:70 | ||||
| chr16:31873648-31873919 | Common:1; Rare:91 | ||||
| chr16:46621312-46621529 | Rare:80 | ||||
| chr16:46689131-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689487-46689708 | Common:2; Rare:88; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46690141-46690270 | Rare:31 | ||||
| chr16:46748218-46748705 | Rare:210 | ||||
| chr16:46763015-46763415 | Common:2; Rare:94 | ||||
| chr16:46789810-46790070 | Common:4; Rare:57 |