| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074626-31074712 | Rare:17 | ||||
| chr16:31094609-31095070 | Common:1; Rare:142; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108224-31108538 | Common:1; Rare:62 | ||||
| chr16:31117475-31117690 | Common:2; Rare:60 | ||||
| chr16:31117861-31118068 | Rare:48 | ||||
| chr16:31142175-31142676 | Common:3; Rare:136 | ||||
| chr16:31179670-31180223 | Common:4; Rare:232; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180510-31180870 | Common:3; Rare:136 | ||||
| chr16:31259930-31259999 | Rare:5 | ||||
| chr16:31442776-31443059 | Common:1; Rare:46 | ||||
| chr16:31458510-31458727 | Common:3; Rare:55 | ||||
| chr16:31458995-31459222 | Common:1; Rare:62 | ||||
| chr16:31459254-31459557 | Common:1; Rare:127 | ||||
| chr16:31459651-31460109 | Common:1; Rare:215 | ||||
| chr16:31508313-31508561 | Common:4; Rare:110 |