| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70114150-70114402 | Common:2; Rare:85 | ||||
| chr16:70346783-70346952 | Common:1; Rare:85 | ||||
| chr16:70523532-70523879 | Common:3; Rare:112; Clinvar (pathogenic):1 | ||||
| chr16:71289205-71289453 | Common:2; Rare:66 | ||||
| chr16:71808761-71808875 | Common:1; Rare:63 | ||||
| chr16:71809034-71809129 | Rare:39 | ||||
| chr16:71845920-71846023 | Common:1; Rare:33 | ||||
| chr16:71895201-71895578 | Common:4; Rare:151 | ||||
| chr16:72093587-72093940 | Rare:88 | ||||
| chr16:74296460-74296987 | Common:1; Rare:175 | ||||
| chr16:74304097-74304393 | Common:2; Rare:62 | ||||
| chr16:75433408-75433812 | Common:4; Rare:121 | ||||
| chr16:75464326-75464454 | Common:4; Rare:55 | ||||
| chr16:75623229-75623390 | Common:3; Rare:55 | ||||
| chr16:75647584-75647829 | Common:2; Rare:120; Clinvar:4; Clinvar (pathogenic):1 |