| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177618708-177619010 | Common:7; Rare:79 | ||||
| chr2:178451090-178451289 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478644 | Common:1; Rare:41 | ||||
| chr2:182426588-182426863 | Common:1; Rare:54 | ||||
| chr2:182426949-182426987 | Rare:10 | ||||
| chr2:182715935-182716376 | Common:3; Rare:148 | ||||
| chr2:186486104-186486344 | Common:3; Rare:78 | ||||
| chr2:186589918-186590034 | Rare:33 | ||||
| chr2:187554228-187554514 | Rare:61 | ||||
| chr2:187554517-187554621 | Common:2; Rare:17 | ||||
| chr2:188974207-188974502 | Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:188974504-188974568 | Rare:18; Clinvar (pathogenic):1 | ||||
| chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr2:189784289-189784540 | Common:4; Rare:91; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:191014074-191014353 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):2 |