| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50450331-50450445 | Rare:45 | ||||
| chr7:50561043-50561247 | Common:1; Rare:50; Clinvar:1 | ||||
| chr7:50782875-50783097 | Common:1; Rare:50 | ||||
| chr7:50792364-50792480 | Rare:23 | ||||
| chr7:50792490-50793104 | Common:7; Rare:279 | ||||
| chr7:50793260-50793740 | Common:2; Rare:159 | ||||
| chr7:54542070-54542520 | Common:3; Rare:121 | ||||
| chr7:54759172-54759393 | Common:2; Rare:101 | ||||
| chr7:55018540-55019180 | Common:3; Rare:171; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55365822-55366062 | Common:1; Rare:96 | ||||
| chr7:55366260-55366421 | Common:1; Rare:65 | ||||
| chr7:55366438-55366910 | Common:5; Rare:240 | ||||
| chr7:55571670-55572110 | Common:1; Rare:115 | ||||
| chr7:55572270-55572760 | Common:4; Rare:152 | ||||
| chr7:55887387-55887488 | Common:1; Rare:29 |