| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:82170177-82170358 | Common:4; Rare:93 | ||||
| chr16:84116801-84117061 | Common:3; Rare:102 | ||||
| chr16:84145123-84145325 | Common:2; Rare:98; Clinvar:4 | ||||
| chr16:84699885-84700053 | Common:2; Rare:70 | ||||
| chr16:85027594-85027844 | Common:1; Rare:137 | ||||
| chr16:85799272-85799745 | Common:3; Rare:150 | ||||
| chr16:86555172-86555313 | Rare:71 | ||||
| chr16:87317326-87317511 | Common:6; Rare:71 | ||||
| chr16:87765919-87766044 | Rare:48 | ||||
| chr16:88570167-88570416 | Common:2; Rare:89 | ||||
| chr16:88663076-88663382 | Common:9; Rare:127 | ||||
| chr16:88856932-88857153 | Common:4; Rare:97; Clinvar (benign):2 | ||||
| chr16:89093800-89093900 | Common:2; Rare:41 | ||||
| chr16:89217627-89217749 | Common:1; Rare:54 | ||||
| chr16:89508313-89508445 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |