| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58733645-58733942 | Common:5; Rare:89 | ||||
| chr16:58734218-58734476 | Common:9; Rare:121 | ||||
| chr16:65122030-65122370 | Common:2; Rare:134 | ||||
| chr16:66426770-66427610 | Common:3; Rare:316 | ||||
| chr16:66516810-66517137 | Rare:82 | ||||
| chr16:66549470-66550010 | Common:8; Rare:231; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66550032-66550244 | Common:4; Rare:166; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:66552403-66552692 | Rare:318 | ||||
| chr16:66552699-66553320 | Common:5; Rare:189 | ||||
| chr16:66603640-66604030 | Rare:55 | ||||
| chr16:66604050-66604320 | Common:3; Rare:79 | ||||
| chr16:66604510-66604756 | Rare:160 | ||||
| chr16:66696604-66697023 | Common:14; Rare:381 | ||||
| chr16:66750332-66751300 | Common:7; Rare:448 | ||||
| chr16:66751531-66751973 | Common:6; Rare:241 |