| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22375088-22375101 | Rare:2 | ||||
| chr16:22436906-22437173 | Rare:95 | ||||
| chr16:22437446-22437623 | Common:2; Rare:50 | ||||
| chr16:23149375-23149801 | Common:2; Rare:133 | ||||
| chr16:23452659-23452819 | Rare:57; Clinvar (benign):1 | ||||
| chr16:23453075-23453274 | Rare:59 | ||||
| chr16:23509879-23509985 | Common:1; Rare:24 | ||||
| chr16:23510355-23510633 | Common:5; Rare:127 | ||||
| chr16:23557043-23557215 | Common:1; Rare:61 | ||||
| chr16:23557216-23557818 | Common:3; Rare:226; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:23596186-23596500 | Common:1; Rare:93 | ||||
| chr16:23641148-23641633 | Common:3; Rare:159; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr16:23678632-23678979 | Common:5; Rare:106 | ||||
| chr16:23835784-23836067 | Common:2; Rare:94 | ||||
| chr16:23836635-23836854 | Common:2; Rare:56 |