| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71426270-71426810 | Common:12; Rare:445 | ||||
| chr16:71572460-71572770 | Common:2; Rare:133; Clinvar (pathogenic):2 | ||||
| chr16:71572780-71573150 | Common:2; Rare:105 | ||||
| chr16:71581560-71582320 | Common:12; Rare:245 | ||||
| chr16:71594060-71594390 | Common:3; Rare:54 | ||||
| chr16:71670540-71670871 | Common:3; Rare:70 | ||||
| chr16:71722900-71723300 | Common:3; Rare:146 | ||||
| chr16:72072973-72073250 | Common:1; Rare:82 | ||||
| chr16:72095917-72096420 | Common:8; Rare:234 | ||||
| chr16:72664926-72665208 | Common:3; Rare:174 | ||||
| chr16:72878560-72878720 | Rare:69 | ||||
| chr16:73057392-73057860 | Common:11; Rare:201 | ||||
| chr16:73058188-73058694 | Common:11; Rare:381 | ||||
| chr16:74368086-74368406 | Common:2; Rare:124 | ||||
| chr16:74508595-74509201 | Common:1; Rare:277 |