| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335601-46335760 | Common:2; Rare:68; Clinvar:7; Clinvar (benign):6 | ||||
| chr22:46762517-46762669 | Common:3; Rare:52 | ||||
| chr22:50783621-50783842 | Common:2; Rare:68 | ||||
| chr3:3126793-3126984 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr3:3179685-3179835 | Common:2; Rare:52 | ||||
| chr3:4493177-4493348 | Rare:60 | ||||
| chr3:8501592-8501854 | Common:1; Rare:101 | ||||
| chr3:9362978-9363098 | Common:1; Rare:45 | ||||
| chr3:9750207-9750301 | Common:1; Rare:36 | ||||
| chr3:9792414-9792570 | Rare:40 | ||||
| chr3:9792777-9793115 | Common:3; Rare:117 | ||||
| chr3:9986777-9987177 | Common:3; Rare:114 | ||||
| chr3:10026302-10026465 | Rare:53 | ||||
| chr3:11846872-11846899 | Rare:5 | ||||
| chr3:12287743-12287963 | Common:6; Rare:43 |