| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:82170151-82170293 | Common:5; Rare:77 | ||||
| chr16:84116801-84117066 | Common:3; Rare:106 | ||||
| chr16:84145099-84145310 | Common:1; Rare:102; Clinvar:3 | ||||
| chr16:84504628-84504832 | Common:5; Rare:86 | ||||
| chr16:85027570-85027828 | Common:2; Rare:147 | ||||
| chr16:85688933-85689188 | Common:7; Rare:94 | ||||
| chr16:86555182-86555327 | Rare:75 | ||||
| chr16:87317311-87317516 | Common:6; Rare:76 | ||||
| chr16:87765908-87766057 | Common:1; Rare:61 | ||||
| chr16:88570167-88570416 | Common:2; Rare:89 | ||||
| chr16:88663070-88663382 | Common:9; Rare:130 | ||||
| chr16:88811891-88812044 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr16:88856816-88857163 | Common:4; Rare:161; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89093766-89093933 | Common:3; Rare:71 | ||||
| chr16:89217627-89217710 | Common:1; Rare:33 |