| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:589505-589659 | Rare:53 | ||||
| chr16:636268-636475 | Common:4; Rare:60 | ||||
| chr16:641744-641950 | Common:3; Rare:71 | ||||
| chr16:642122-642452 | Common:1; Rare:108 | ||||
| chr16:649015-649404 | Common:3; Rare:112 | ||||
| chr16:680309-680537 | Common:2; Rare:76 | ||||
| chr16:680646-680654 | Rare:3 | ||||
| chr16:681153-681548 | Rare:127; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr16:684326-684501 | Common:3; Rare:100 | ||||
| chr16:695314-695436 | Common:3; Rare:55 | ||||
| chr16:721069-721162 | Common:2; Rare:22 | ||||
| chr16:740968-741160 | Rare:59 | ||||
| chr16:970823-971201 | Common:7; Rare:170 | ||||
| chr16:1351872-1351974 | Common:1; Rare:49; Clinvar:5; Clinvar (benign):1 | ||||
| chr16:1420707-1420962 | Common:1; Rare:106 |