| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85611842-85612191 | Rare:349 | ||||
| chr2:85615963-85616393 | Common:6; Rare:444 | ||||
| chr2:85616625-85617137 | Common:13; Rare:183 | ||||
| chr2:85753373-85753940 | Common:4; Rare:220 | ||||
| chr2:85753875-85754210 | Rare:134 | ||||
| chr2:85754550-85755120 | Common:11; Rare:399 | ||||
| chr2:85888727-85889570 | Common:13; Rare:435; Clinvar:7; Clinvar (benign):8 | ||||
| chr2:86105762-86106328 | Common:10; Rare:528 | ||||
| chr2:86194920-86195225 | Common:2; Rare:180 | ||||
| chr2:86195369-86195720 | Common:22; Rare:267 | ||||
| chr2:86199332-86199616 | Common:4; Rare:185 | ||||
| chr2:86254846-86255250 | Rare:139 | ||||
| chr2:86336748-86337195 | Common:5; Rare:196 | ||||
| chr2:86337511-86337863 | Common:1; Rare:174; Clinvar (benign):2 | ||||
| chr2:86440610-86440955 | Common:8; Rare:251 |