| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31073373-31073506 | Rare:43 | ||||
| chr16:31073641-31073889 | Rare:72 | ||||
| chr16:31074164-31074469 | Common:2; Rare:87 | ||||
| chr16:31074622-31074857 | Common:2; Rare:45 | ||||
| chr16:31094484-31095040 | Common:1; Rare:174; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108272-31108509 | Rare:50 | ||||
| chr16:31117456-31117713 | Common:2; Rare:77 | ||||
| chr16:31117798-31118092 | Rare:70 | ||||
| chr16:31130688-31130897 | Rare:34 | ||||
| chr16:31130936-31131237 | Common:4; Rare:79 | ||||
| chr16:31135064-31135203 | Rare:45 | ||||
| chr16:31135653-31135851 | Rare:48 | ||||
| chr16:31136099-31136261 | Common:2; Rare:30 | ||||
| chr16:31142188-31142662 | Common:2; Rare:127 | ||||
| chr16:31179662-31180234 | Common:4; Rare:236; Clinvar:2; Clinvar (benign):2 |