| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:81006798-81007272 | Common:5; Rare:160 | ||||
| chr16:81314771-81315071 | Common:3; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:84116750-84117057 | Common:4; Rare:120 | ||||
| chr16:84504608-84504861 | Common:8; Rare:109 | ||||
| chr16:84699891-84700049 | Common:2; Rare:67 | ||||
| chr16:85027613-85027813 | Common:1; Rare:106 | ||||
| chr16:85799323-85799760 | Common:3; Rare:134 | ||||
| chr16:87317359-87317502 | Common:5; Rare:52 | ||||
| chr16:87765906-87766017 | Rare:46 | ||||
| chr16:87951213-87951502 | Common:2; Rare:105 | ||||
| chr16:88570174-88570436 | Common:1; Rare:96 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88706221-88706553 | Common:4; Rare:148 | ||||
| chr16:88732494-88732703 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:88856762-88857163 | Common:4; Rare:187; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 |