| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74606937-74607206 | Rare:133 | ||||
| chr16:74666809-74667212 | Common:8; Rare:131 | ||||
| chr16:74985046-74985291 | Common:2; Rare:82 | ||||
| chr16:75433368-75433787 | Common:4; Rare:136 | ||||
| chr16:75464379-75464464 | Common:2; Rare:38 | ||||
| chr16:75464646-75464918 | Common:3; Rare:90 | ||||
| chr16:75495402-75495571 | Common:2; Rare:66 | ||||
| chr16:75556220-75556251 | Rare:16; Clinvar (benign):1 | ||||
| chr16:75556253-75556360 | Common:1; Rare:31; Clinvar (benign):2 | ||||
| chr16:75647578-75647788 | Common:1; Rare:103; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190685-77191015 | Common:10; Rare:109 | ||||
| chr16:77191089-77191224 | Common:2; Rare:56 | ||||
| chr16:81006820-81007272 | Common:4; Rare:150 | ||||
| chr16:81314744-81315129 | Common:3; Rare:184; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:82170176-82170249 | Common:3; Rare:36 |