| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89701623-89701833 | Common:1; Rare:77 | ||||
| chr16:89720836-89721004 | Common:1; Rare:48 | ||||
| chr16:89816613-89816803 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873482-89873854 | Common:3; Rare:167 | ||||
| chr16:89883132-89883456 | Common:1; Rare:117 | ||||
| chr16:89918703-89918918 | Common:5; Rare:64; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:89921601-89921953 | Common:1; Rare:91 | ||||
| chr16:89972423-89972662 | Common:1; Rare:88 | ||||
| chr16:90019403-90019660 | Common:5; Rare:78 | ||||
| chr16:90019807-90019989 | Rare:57 | ||||
| chr16:90022533-90022713 | Rare:71 | ||||
| chr17:352278-352618 | Common:3; Rare:81 | ||||
| chr17:352703-353268 | Common:8; Rare:115 | ||||
| chr17:409990-410420 | Common:9; Rare:194 | ||||
| chr17:714699-714962 | Common:4; Rare:91; Clinvar (benign):1 |