| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184734050-184734403 | Common:5; Rare:128 | ||||
| chr4:184805529-184805859 | Common:2; Rare:57 | ||||
| chr4:185396580-185396845 | Rare:85 | ||||
| chr4:185396877-185397058 | Rare:72 | ||||
| chr4:185425870-185426029 | Common:2; Rare:58 | ||||
| chr4:185535352-185535632 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186723783-186723953 | Common:4; Rare:65 | ||||
| chr4:189940613-189941001 | Common:14; Rare:136 | ||||
| chr5:218112-218409 | Common:3; Rare:119; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443095-443272 | Common:9; Rare:79 | ||||
| chr5:612190-612346 | Rare:60 | ||||
| chr5:892698-892923 | Common:5; Rare:82 | ||||
| chr5:1799795-1799988 | Common:4; Rare:92 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378498-6378699 | Rare:81 |