| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130440994-130441291 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130486650-130486980 | Common:7; Rare:115 | ||||
| chr7:131109410-131110276 | Common:7; Rare:237 | ||||
| chr7:131110333-131110487 | Common:2; Rare:18 | ||||
| chr7:131327321-131327438 | Rare:23 | ||||
| chr7:131327688-131327941 | Rare:154 | ||||
| chr7:131327960-131328300 | Common:1; Rare:157 | ||||
| chr7:131328218-131328481 | Common:1; Rare:66 | ||||
| chr7:131556315-131556826 | Common:11; Rare:236 | ||||
| chr7:133252874-133253132 | Rare:170 | ||||
| chr7:134316831-134317212 | Common:4; Rare:197 | ||||
| chr7:134448614-134449120 | Common:6; Rare:170 | ||||
| chr7:134451455-134452051 | Common:1; Rare:269 | ||||
| chr7:134459003-134459182 | Common:1; Rare:89 | ||||
| chr7:134646534-134646881 | Common:14; Rare:197 |