| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4371688-4371861 | Rare:63 | ||||
| chr16:4425744-4425964 | Common:1; Rare:115 | ||||
| chr16:4476273-4476556 | Common:3; Rare:96 | ||||
| chr16:4507567-4507880 | Common:1; Rare:88 | ||||
| chr16:4538394-4538609 | Common:2; Rare:73 | ||||
| chr16:4614783-4615047 | Common:1; Rare:88 | ||||
| chr16:4693429-4693747 | Common:3; Rare:144 | ||||
| chr16:4734128-4734541 | Common:1; Rare:138 | ||||
| chr16:4767097-4767306 | Common:2; Rare:73 | ||||
| chr16:4795351-4795506 | Common:1; Rare:54 | ||||
| chr16:4802586-4802866 | Rare:100; Clinvar:5 | ||||
| chr16:4847226-4847429 | Common:1; Rare:88 | ||||
| chr16:4870392-4870549 | Common:1; Rare:61 | ||||
| chr16:5033920-5033968 | Rare:19 | ||||
| chr16:5071778-5071861 | Rare:39; Clinvar (benign):1 |