| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94297343-94297631 | Rare:55 | ||||
| chr7:94392139-94392313 | Common:2; Rare:24 | ||||
| chr7:94395579-94396038 | Common:4; Rare:79 | ||||
| chr7:94396155-94396178 | Rare:2 | ||||
| chr7:94396825-94396988 | Rare:28 | ||||
| chr7:94397720-94397777 | Common:1; Rare:20; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:94397879-94398160 | Common:1; Rare:33 | ||||
| chr7:94404541-94404903 | Rare:92; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94406247-94406345 | Common:1; Rare:26; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94406723-94406896 | Rare:38 | ||||
| chr7:94407840-94407940 | Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:94408163-94408380 | Common:1; Rare:58; Clinvar:3 | ||||
| chr7:94408766-94409021 | Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:94409311-94409644 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:94409973-94410607 | Common:3; Rare:133; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 |