| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:86520910-86521237 | Common:4; Rare:64 | ||||
| chr1:86548933-86549238 | Common:3; Rare:56 | ||||
| chr1:86549405-86549600 | Common:1; Rare:31 | ||||
| chr1:86558700-86558993 | Common:4; Rare:60 | ||||
| chr1:86561778-86562109 | Common:1; Rare:64 | ||||
| chr1:86566285-86566602 | Rare:46 | ||||
| chr1:86568758-86569116 | Common:1; Rare:68 | ||||
| chr1:86574429-86574915 | Common:1; Rare:97 | ||||
| chr1:89009017-89009299 | Common:1; Rare:62 | ||||
| chr1:89009599-89009768 | Rare:29 | ||||
| chr1:90219650-90219791 | Common:2; Rare:55 | ||||
| chr1:90851588-90851809 | Common:2; Rare:56 | ||||
| chr1:92837155-92837633 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:93575749-93575853 | Rare:21 | ||||
| chr1:93591681-93592026 | Common:1; Rare:56 |