| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130205373-130205599 | Rare:92 | ||||
| chr7:130440977-130441344 | Common:3; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130491965-130492270 | Common:1; Rare:80 | ||||
| chr7:131327686-131327909 | Rare:67 | ||||
| chr7:131556271-131556375 | Common:1; Rare:35 | ||||
| chr7:132576445-132576580 | Common:2; Rare:35 | ||||
| chr7:134127082-134127370 | Rare:74 | ||||
| chr7:134316841-134317175 | Common:2; Rare:96 | ||||
| chr7:134646553-134646934 | Common:10; Rare:125 | ||||
| chr7:134986372-134986577 | Common:4; Rare:77 | ||||
| chr7:135170413-135170826 | Common:3; Rare:151 | ||||
| chr7:135211486-135211684 | Common:2; Rare:95 | ||||
| chr7:135662348-135662547 | Common:4; Rare:89 | ||||
| chr7:135977062-135977487 | Common:3; Rare:155 | ||||
| chr7:136868422-136869294 | Common:5; Rare:176; Clinvar (benign):3 |