| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4425767-4425923 | Common:1; Rare:85 | ||||
| chr16:4476257-4476499 | Common:3; Rare:86 | ||||
| chr16:4538414-4538538 | Common:1; Rare:38 | ||||
| chr16:4538714-4538994 | Rare:101 | ||||
| chr16:4693437-4693731 | Common:2; Rare:128 | ||||
| chr16:4734199-4734531 | Common:1; Rare:108 | ||||
| chr16:4767114-4767341 | Common:2; Rare:76 | ||||
| chr16:4795336-4795446 | Rare:39 | ||||
| chr16:4795722-4795953 | Common:1; Rare:99 | ||||
| chr16:4800496-4800942 | Rare:154; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr16:4802594-4802967 | Common:1; Rare:150; Clinvar:8; Clinvar (benign):1 | ||||
| chr16:4846189-4846477 | Common:2; Rare:82 | ||||
| chr16:4847239-4847471 | Common:1; Rare:103 | ||||
| chr16:5033920-5033968 | Rare:19 | ||||
| chr16:5097737-5098041 | Common:4; Rare:101 |