| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29996064-29996296 | Common:2; Rare:82 | ||||
| chr16:30064279-30064480 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr16:30065463-30065885 | Rare:137 | ||||
| chr16:30069660-30069937 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:30075889-30076059 | Common:1; Rare:57 | ||||
| chr16:30123043-30123342 | Common:5; Rare:87 | ||||
| chr16:30355219-30355434 | Common:1; Rare:76 | ||||
| chr16:30355795-30355938 | Common:1; Rare:34 | ||||
| chr16:30374714-30374802 | Rare:18 | ||||
| chr16:30445871-30445931 | Rare:22 | ||||
| chr16:30527281-30527562 | Rare:76 | ||||
| chr16:30534828-30535070 | Common:2; Rare:75 | ||||
| chr16:30585537-30585897 | Common:1; Rare:81 | ||||
| chr16:30650745-30650971 | Rare:70 | ||||
| chr16:30698037-30698246 | Common:1; Rare:105 |