| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905494-84905980 | Common:2; Rare:147 | ||||
| chr2:84906997-84907366 | Common:1; Rare:71 | ||||
| chr2:85327887-85328092 | Common:3; Rare:96 | ||||
| chr2:85354511-85354818 | Common:1; Rare:102 | ||||
| chr2:85410334-85410411 | Rare:14 | ||||
| chr2:85413994-85414098 | Common:1; Rare:23 | ||||
| chr2:85418440-85418764 | Common:4; Rare:83 | ||||
| chr2:85539068-85539227 | Common:3; Rare:80 | ||||
| chr2:85561432-85561621 | Common:1; Rare:64; Clinvar:4 | ||||
| chr2:85595534-85595809 | Common:2; Rare:92 | ||||
| chr2:85602635-85602915 | Rare:71 | ||||
| chr2:85612001-85612158 | Rare:54 | ||||
| chr2:85616022-85616350 | Common:2; Rare:132 | ||||
| chr2:86105743-86106277 | Common:3; Rare:170 |