| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69424485-69424733 | Common:1; Rare:76 | ||||
| chr16:69726442-69726812 | Common:3; Rare:96 | ||||
| chr16:69762266-69762387 | Common:1; Rare:29 | ||||
| chr16:70114127-70114369 | Common:3; Rare:88 | ||||
| chr16:70289419-70289802 | Common:3; Rare:151; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70346785-70346942 | Common:1; Rare:80 | ||||
| chr16:70523533-70523855 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
| chr16:71808778-71808869 | Common:1; Rare:52 | ||||
| chr16:71809042-71809348 | Common:3; Rare:99 | ||||
| chr16:71845885-71846017 | Common:2; Rare:43 | ||||
| chr16:71895241-71895578 | Common:3; Rare:132 | ||||
| chr16:72008517-72008760 | Common:5; Rare:86; Clinvar (benign):1 | ||||
| chr16:72093579-72093986 | Common:1; Rare:103 | ||||
| chr16:74296719-74296941 | Rare:94 | ||||
| chr16:74607080-74607197 | Rare:61 |