| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187737938-187738139 | Common:2; Rare:33 | ||||
| chr3:188152902-188153038 | Common:1; Rare:22 | ||||
| chr3:188153281-188153598 | Common:1; Rare:52 | ||||
| chr3:188153791-188154230 | Common:1; Rare:110 | ||||
| chr3:190120309-190120688 | Common:1; Rare:160; Clinvar (pathogenic):1 | ||||
| chr3:190120791-190120972 | Rare:49 | ||||
| chr3:190120976-190121004 | Rare:7 | ||||
| chr3:190513903-190514162 | Common:2; Rare:67 | ||||
| chr3:191329241-191329717 | Common:4; Rare:146 | ||||
| chr3:192917850-192918008 | Common:2; Rare:70 | ||||
| chr3:193593095-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194487008-194487172 | Common:3; Rare:74 | ||||
| chr3:194672140-194672471 | Common:1; Rare:105 | ||||
| chr3:195271071-195271302 | Common:1; Rare:93 | ||||
| chr3:195442295-195442420 | Common:1; Rare:34 |