| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84116806-84117066 | Common:3; Rare:103 | ||||
| chr16:84145105-84145259 | Rare:85 | ||||
| chr16:84699766-84700053 | Common:2; Rare:122 | ||||
| chr16:85613091-85613368 | Common:1; Rare:106 | ||||
| chr16:85799368-85799760 | Common:3; Rare:120 | ||||
| chr16:86555190-86555329 | Rare:71 | ||||
| chr16:87317348-87317527 | Common:5; Rare:73 | ||||
| chr16:87765911-87766017 | Rare:44 | ||||
| chr16:88570155-88570436 | Common:2; Rare:102 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88856932-88857163 | Common:4; Rare:103; Clinvar (benign):2 | ||||
| chr16:89560546-89560724 | Rare:78 | ||||
| chr16:89657644-89657799 | Common:1; Rare:78 | ||||
| chr16:89686587-89686708 | Common:6; Rare:58 | ||||
| chr16:89816621-89816823 | Common:5; Rare:105; Clinvar:2; Clinvar (benign):1 |