| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606784-44607094 | Common:2; Rare:96 | ||||
| chr7:44759333-44759655 | Rare:80 | ||||
| chr7:44760063-44760451 | Common:1; Rare:134 | ||||
| chr7:44796381-44796692 | Common:2; Rare:113 | ||||
| chr7:44797531-44797573 | Rare:7 | ||||
| chr7:44848132-44848479 | Common:2; Rare:87 | ||||
| chr7:44999564-44999768 | Common:4; Rare:71 | ||||
| chr7:44999958-45000357 | Common:1; Rare:97; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45111655-45111822 | Common:1; Rare:67 | ||||
| chr7:47280158-47280364 | Common:1; Rare:53 | ||||
| chr7:47539594-47539888 | Common:3; Rare:57 | ||||
| chr7:48089064-48089281 | Common:2; Rare:59 | ||||
| chr7:50450314-50450460 | Common:1; Rare:61 | ||||
| chr7:55018909-55019240 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55019305-55019361 | Rare:18 |