| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:47979500-47979742 | Rare:89 | ||||
| chr7:48088861-48089245 | Common:4; Rare:93 | ||||
| chr7:50450302-50450541 | Common:1; Rare:107 | ||||
| chr7:50783105-50783157 | Rare:20 | ||||
| chr7:54542029-54542714 | Common:4; Rare:167 | ||||
| chr7:55365669-55365960 | Common:1; Rare:113 | ||||
| chr7:55366263-55366408 | Common:1; Rare:59 | ||||
| chr7:55516035-55516133 | Common:1; Rare:25 | ||||
| chr7:55572278-55572617 | Common:1; Rare:119 | ||||
| chr7:55887387-55887674 | Common:5; Rare:98 | ||||
| chr7:55951780-55951935 | Rare:47 | ||||
| chr7:56034137-56034294 | Rare:49 | ||||
| chr7:56051429-56051931 | Common:1; Rare:184; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064177-56064367 | Common:2; Rare:117 | ||||
| chr7:56106395-56106713 | Common:9; Rare:112 |