| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2669561-2669809 | Common:5; Rare:61 | ||||
| chr16:2669999-2670273 | Common:4; Rare:84 | ||||
| chr16:2673311-2673705 | Common:10; Rare:141 | ||||
| chr16:3021615-3021918 | Common:1; Rare:93 | ||||
| chr16:3031056-3031362 | Common:3; Rare:84 | ||||
| chr16:3150513-3150829 | Common:4; Rare:175 | ||||
| chr16:3672344-3672644 | Common:2; Rare:81 | ||||
| chr16:4797938-4798139 | Rare:112; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:8822786-8822851 | Rare:9 | ||||
| chr16:8923322-8923634 | Common:1; Rare:88 | ||||
| chr16:10451698-10451836 | Rare:34 | ||||
| chr16:10898679-10898947 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:11885179-11885569 | Rare:77 | ||||
| chr16:11887714-11887794 | Rare:17 | ||||
| chr16:11896641-11896883 | Common:1; Rare:64 |