| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30610127-30610231 | Common:1; Rare:16 | ||||
| chr16:30610301-30610321 | Rare:5 | ||||
| chr16:30610373-30610428 | Rare:17 | ||||
| chr16:30650714-30650966 | Rare:74 | ||||
| chr16:30657890-30658258 | Common:1; Rare:95 | ||||
| chr16:30658289-30658515 | Common:1; Rare:60 | ||||
| chr16:30658585-30658849 | Common:1; Rare:82 | ||||
| chr16:30661235-30661364 | Rare:35 | ||||
| chr16:30662195-30662461 | Common:1; Rare:64 | ||||
| chr16:30664602-30664729 | Rare:30 | ||||
| chr16:30698029-30698208 | Common:1; Rare:84 | ||||
| chr16:30698213-30698260 | Rare:18 | ||||
| chr16:30698400-30698739 | Common:1; Rare:131 | ||||
| chr16:30698979-30699379 | Rare:112; Clinvar (benign):1 | ||||
| chr16:30748128-30748447 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 |