| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:28958318-28958429 | Rare:28 | ||||
| chr7:29989656-29989952 | Rare:116 | ||||
| chr7:30026626-30026862 | Rare:55 | ||||
| chr7:30134862-30135181 | Common:4; Rare:109 | ||||
| chr7:30284262-30284432 | Common:1; Rare:65 | ||||
| chr7:30504740-30505079 | Common:3; Rare:113 | ||||
| chr7:30594711-30595076 | Common:7; Rare:167; Clinvar:8; Clinvar (benign):14 | ||||
| chr7:31687176-31687236 | Rare:20 | ||||
| chr7:32490301-32490462 | Common:1; Rare:54 | ||||
| chr7:32495240-32495624 | Common:1; Rare:98 | ||||
| chr7:32495876-32496011 | Rare:30 | ||||
| chr7:33062588-33063197 | Common:5; Rare:215 | ||||
| chr7:33129198-33129587 | Common:5; Rare:115 | ||||
| chr7:35695133-35695257 | Common:1; Rare:42 | ||||
| chr7:35800721-35801295 | Common:3; Rare:220 |