| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:41963550-41964070 | Common:1; Rare:113 | ||||
| chr2:41964133-41964314 | Common:2; Rare:40 | ||||
| chr2:42030357-42030629 | Common:4; Rare:75 | ||||
| chr2:42045547-42046565 | Common:6; Rare:251 | ||||
| chr2:42046810-42047190 | Common:3; Rare:78 | ||||
| chr2:42050363-42050763 | Common:4; Rare:141 | ||||
| chr2:42051140-42051430 | Common:2; Rare:63 | ||||
| chr2:42053121-42053842 | Common:5; Rare:330; Clinvar (pathogenic):2 | ||||
| chr2:42141570-42142180 | Common:2; Rare:130 | ||||
| chr2:42809780-42810240 | Common:2; Rare:153 | ||||
| chr2:42810370-42810636 | Common:1; Rare:141 | ||||
| chr2:42811265-42811457 | Rare:53 | ||||
| chr2:42845100-42845640 | Common:2; Rare:136 | ||||
| chr2:42923968-42925173 | Common:15; Rare:401 | ||||
| chr2:43041928-43042258 | Common:2; Rare:61 |