| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126784-3127067 | Common:4; Rare:115; Clinvar (benign):4 | ||||
| chr3:9362814-9363099 | Common:2; Rare:86 | ||||
| chr3:9397436-9397615 | Rare:60 | ||||
| chr3:9749789-9749963 | Rare:50 | ||||
| chr3:9792376-9792610 | Rare:64 | ||||
| chr3:9792746-9793127 | Common:3; Rare:132 | ||||
| chr3:9933673-9933860 | Common:1; Rare:72 | ||||
| chr3:10026283-10026437 | Common:1; Rare:53 | ||||
| chr3:10292895-10293003 | Common:1; Rare:23 | ||||
| chr3:11225854-11225999 | Rare:22 | ||||
| chr3:11272190-11272422 | Common:2; Rare:57 | ||||
| chr3:12484325-12484520 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664101-12664330 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124728-14125185 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178505-14178857 | Common:3; Rare:177; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 |