| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726382-69726868 | Common:7; Rare:209 | ||||
| chr16:69754864-69755094 | Common:1; Rare:95 | ||||
| chr16:69762250-69762394 | Common:3; Rare:71 | ||||
| chr16:70114089-70114627 | Common:8; Rare:264 | ||||
| chr16:70173438-70173561 | Rare:20 | ||||
| chr16:70262356-70262851 | Common:6; Rare:242; Clinvar:16; Clinvar (benign):6 | ||||
| chr16:70289390-70289790 | Common:6; Rare:314; Clinvar:2; Clinvar (benign):8 | ||||
| chr16:70299092-70299270 | Common:2; Rare:75 | ||||
| chr16:70346751-70346989 | Common:2; Rare:119 | ||||
| chr16:70438986-70439458 | Common:4; Rare:301 | ||||
| chr16:70454324-70454638 | Common:3; Rare:155 | ||||
| chr16:70523456-70523868 | Common:6; Rare:281; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:70679401-70680040 | Common:3; Rare:312 | ||||
| chr16:70685847-70686242 | Common:7; Rare:216 | ||||
| chr16:70801008-70801356 | Common:5; Rare:192 |