| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30541172-30541387 | Common:1; Rare:30 | ||||
| chr16:30634265-30634562 | Common:1; Rare:74 | ||||
| chr16:30768505-30768736 | Rare:77 | ||||
| chr16:30875328-30875490 | Rare:54 | ||||
| chr16:30892699-30893002 | Common:1; Rare:95 | ||||
| chr16:31477100-31477468 | Common:1; Rare:106 | ||||
| chr16:47598996-47599035 | Rare:12 | ||||
| chr16:51151974-51152125 | Common:2; Rare:29 | ||||
| chr16:52532535-52532849 | Common:3; Rare:56 | ||||
| chr16:52565035-52565344 | Common:4; Rare:57 | ||||
| chr16:55485340-55485774 | Common:2; Rare:128; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:56269371-56269509 | Common:1; Rare:43 | ||||
| chr16:56617439-56617572 | Common:2; Rare:29 | ||||
| chr16:57172852-57172890 | Rare:8 | ||||
| chr16:57206439-57206494 | Rare:12 |