| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32570645-32571048 | Common:1; Rare:173 | ||||
| chr3:32685074-32685470 | Rare:111 | ||||
| chr3:33097090-33097316 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33113876-33113983 | Common:2; Rare:32 | ||||
| chr3:33218772-33219025 | Common:3; Rare:77 | ||||
| chr3:33277289-33277487 | Common:2; Rare:53 | ||||
| chr3:33440907-33441099 | Rare:41 | ||||
| chr3:33645452-33645521 | Rare:8 | ||||
| chr3:33658990-33659231 | Common:3; Rare:49 | ||||
| chr3:33659505-33659785 | Common:1; Rare:64 | ||||
| chr3:33718061-33718314 | Rare:95 | ||||
| chr3:33798477-33798681 | Common:2; Rare:73 | ||||
| chr3:36380193-36380674 | Common:5; Rare:156 | ||||
| chr3:36993073-36993595 | Common:2; Rare:185; Clinvar:37; Clinvar (benign):17; Clinvar (pathogenic):4 | ||||
| chr3:36993724-36993867 | Rare:54 |