| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88720183-88720665 | Common:9; Rare:416; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88785039-88785400 | Common:8; Rare:320 | ||||
| chr16:88785430-88785858 | Rare:198 | ||||
| chr16:88803502-88803908 | Common:16; Rare:448; Clinvar (benign):1 | ||||
| chr16:88803936-88804663 | Common:7; Rare:511; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:88804568-88804760 | Rare:186; Clinvar (benign):2 | ||||
| chr16:88810666-88811171 | Common:9; Rare:169 | ||||
| chr16:88811502-88811669 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88811620-88811820 | Common:4; Rare:66; Clinvar (benign):2 | ||||
| chr16:88811832-88812221 | Common:6; Rare:377; Clinvar (benign):3 | ||||
| chr16:88812157-88812660 | Common:16; Rare:293 | ||||
| chr16:88856858-88857240 | Common:12; Rare:522; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:88940590-88941080 | Common:2; Rare:231 | ||||
| chr16:88941094-88941480 | Rare:204 | ||||
| chr16:88941780-88941994 | Common:4; Rare:130 |