| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5190105-5190307 | Rare:164 | ||||
| chr7:5423670-5424061 | Common:7; Rare:166 | ||||
| chr7:5425300-5425710 | Rare:124 | ||||
| chr7:5513736-5513897 | Common:2; Rare:135 | ||||
| chr7:5513980-5514470 | Common:6; Rare:184 | ||||
| chr7:5527590-5528210 | Common:6; Rare:211; Clinvar:1; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr7:5529813-5530213 | Common:6; Rare:320 | ||||
| chr7:5530525-5530823 | Common:2; Rare:183; Clinvar (benign):3 | ||||
| chr7:5562714-5562908 | Rare:78 | ||||
| chr7:5592662-5592884 | Common:2; Rare:139 | ||||
| chr7:5594179-5594579 | Common:8; Rare:198 | ||||
| chr7:5781555-5781753 | Common:1; Rare:148 | ||||
| chr7:6009017-6009407 | Common:4; Rare:165; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr7:6058991-6059324 | Common:9; Rare:208 | ||||
| chr7:6104587-6105043 | Common:10; Rare:329 |