| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11976604-11976760 | Common:3; Rare:62 | ||||
| chr16:14632722-14632989 | Common:1; Rare:89 | ||||
| chr16:15094251-15094376 | Rare:59 | ||||
| chr16:15888587-15888815 | Common:2; Rare:82 | ||||
| chr16:18801536-18801872 | Common:4; Rare:101 | ||||
| chr16:18925793-18925922 | Common:1; Rare:42 | ||||
| chr16:19067825-19067904 | Common:1; Rare:19 | ||||
| chr16:20806355-20806617 | Rare:91 | ||||
| chr16:20900525-20900873 | Common:2; Rare:84 | ||||
| chr16:21158523-21158718 | Common:1; Rare:57 | ||||
| chr16:21953028-21953423 | Common:1; Rare:100; Clinvar (benign):3 | ||||
| chr16:22437184-22437275 | Rare:29 | ||||
| chr16:22437513-22437667 | Common:2; Rare:39 | ||||
| chr16:23557315-23557578 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641545 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 |