| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100100011-100100375 | Common:1; Rare:161 | ||||
| chr7:100100498-100100814 | Rare:137 | ||||
| chr7:100101274-100101750 | Common:1; Rare:192; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100119255-100119758 | Common:1; Rare:156; Clinvar:1 | ||||
| chr7:100119856-100119945 | Rare:32 | ||||
| chr7:100126658-100126993 | Common:1; Rare:96 | ||||
| chr7:100148674-100149040 | Common:1; Rare:161 | ||||
| chr7:100155326-100155587 | Common:1; Rare:53 | ||||
| chr7:100428652-100428968 | Common:4; Rare:118 | ||||
| chr7:100429094-100429467 | Common:4; Rare:164 | ||||
| chr7:100429539-100429806 | Common:2; Rare:93 | ||||
| chr7:100539051-100539261 | Common:1; Rare:55 | ||||
| chr7:100586116-100586456 | Common:3; Rare:109 | ||||
| chr7:100604213-100604488 | Common:1; Rare:62 | ||||
| chr7:100673748-100673879 | Common:3; Rare:68 |