| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74172695-74172989 | Common:1; Rare:81 | ||||
| chr2:74293707-74293929 | Rare:51 | ||||
| chr2:74370464-74370827 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:74377432-74377724 | Common:1; Rare:73 | ||||
| chr2:74856267-74856550 | Common:1; Rare:61 | ||||
| chr2:75667709-75667970 | Common:2; Rare:51 | ||||
| chr2:85343416-85343473 | Rare:8 | ||||
| chr2:85542326-85543043 | Common:3; Rare:180; Clinvar:1; Clinvar (benign):12 | ||||
| chr2:85543565-85543780 | Rare:36; Clinvar (benign):1 | ||||
| chr2:85596478-85596537 | Common:1; Rare:20 | ||||
| chr2:86153558-86153764 | Rare:38 | ||||
| chr2:86158597-86158958 | Common:5; Rare:76 | ||||
| chr2:86207114-86207253 | Common:1; Rare:40 | ||||
| chr2:86480908-86481173 | Rare:57 | ||||
| chr2:86482265-86482690 | Common:1; Rare:102 |