| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31202658-31202984 | Common:2; Rare:114 | ||||
| chr16:31355035-31355236 | Common:1; Rare:57 | ||||
| chr16:31442744-31443059 | Common:1; Rare:53 | ||||
| chr16:31458891-31459161 | Rare:78 | ||||
| chr16:31459296-31459517 | Common:1; Rare:90 | ||||
| chr16:31471901-31472200 | Rare:69 | ||||
| chr16:31508365-31508490 | Common:4; Rare:52 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46789925-46790084 | Common:4; Rare:40 | ||||
| chr16:46973532-46973761 | Rare:89 | ||||
| chr16:47461035-47461374 | Common:2; Rare:129; Clinvar (benign):2 | ||||
| chr16:48244260-48244575 | Common:2; Rare:95 | ||||
| chr16:48385258-48385522 | Common:3; Rare:102 | ||||
| chr16:50245942-50246178 | Common:2; Rare:57 | ||||
| chr16:50681279-50681416 | Rare:27 |