| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188316918-188317228 | Common:1; Rare:40 | ||||
| chr3:188342315-188342320 | Rare:1 | ||||
| chr3:188383002-188383051 | Rare:14 | ||||
| chr3:188536205-188536305 | Rare:22 | ||||
| chr3:188862487-188862584 | Rare:12 | ||||
| chr3:188903977-188904101 | Common:3; Rare:19 | ||||
| chr3:190112968-190113043 | Rare:15 | ||||
| chr3:190113411-190113687 | Common:4; Rare:42 | ||||
| chr3:190119542-190119913 | Common:4; Rare:63 | ||||
| chr3:191380686-191380931 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):4 | ||||
| chr3:192917538-192917563 | Common:2; Rare:5 | ||||
| chr3:194135078-194135223 | Rare:46 | ||||
| chr3:194406069-194406393 | Common:1; Rare:84 | ||||
| chr3:194406695-194406784 | Rare:20 | ||||
| chr3:194407576-194407707 | Common:1; Rare:29 |