| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241686662-241687563 | Common:30; Rare:944 | ||||
| chr2:241701272-241701672 | Common:7; Rare:148 | ||||
| chr2:241701794-241702194 | Common:6; Rare:505 | ||||
| chr2:241702484-241702810 | Common:8; Rare:154 | ||||
| chr2:241734301-241734754 | Common:61; Rare:931; Clinvar:19; Clinvar (benign):5 | ||||
| chr2:241735410-241735980 | Common:9; Rare:323; Clinvar:7; Clinvar (benign):6 | ||||
| chr2:241813675-241814075 | Common:1; Rare:60 | ||||
| chr2:241858740-241859150 | Common:3; Rare:208 | ||||
| chr20:290352-290623 | Common:26; Rare:137 | ||||
| chr20:290742-290855 | Common:1; Rare:24 | ||||
| chr20:297080-297760 | Common:19; Rare:426 | ||||
| chr20:324761-325161 | Common:2; Rare:73 | ||||
| chr20:325207-325643 | Common:1; Rare:654 | ||||
| chr20:325666-325943 | Rare:193 | ||||
| chr20:346470-346904 | Common:7; Rare:319 |