| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10973762-10973950 | Rare:81 | ||||
| chr7:12211151-12211354 | Common:3; Rare:97 | ||||
| chr7:16645807-16646196 | Common:3; Rare:124 | ||||
| chr7:17940449-17940606 | Common:2; Rare:69 | ||||
| chr7:20217329-20217595 | Common:1; Rare:57 | ||||
| chr7:21427797-21428093 | Common:3; Rare:113 | ||||
| chr7:21945820-21946245 | Common:3; Rare:135 | ||||
| chr7:22822766-22822954 | Common:3; Rare:69 | ||||
| chr7:23014119-23014356 | Common:3; Rare:66 | ||||
| chr7:23105667-23105804 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:23181869-23182135 | Common:1; Rare:115 | ||||
| chr7:23467956-23468071 | Common:1; Rare:23 | ||||
| chr7:23470334-23470560 | Rare:70 | ||||
| chr7:23531948-23532083 | Common:1; Rare:54 | ||||
| chr7:23597266-23597412 | Rare:46 |