| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:159100310-159100509 | Common:3; Rare:63 | ||||
| chr5:180831600-180831752 | Common:3; Rare:58 | ||||
| chr6:4018683-4018835 | Common:2; Rare:52 | ||||
| chr6:10801946-10802214 | Rare:72; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:21593575-21593792 | Rare:62 | ||||
| chr6:22146202-22146347 | Rare:33 | ||||
| chr6:26122996-26123193 | Common:2; Rare:56 | ||||
| chr6:27772768-27772993 | Common:2; Rare:22 | ||||
| chr6:57961358-57961653 | Common:2; Rare:89 | ||||
| chr6:85678729-85678955 | Rare:70 | ||||
| chr6:122833311-122833375 | Common:1; Rare:5 | ||||
| chr7:32728737-32728823 | Common:4; Rare:25 | ||||
| chr7:44467579-44467852 | Common:2; Rare:46 | ||||
| chr7:44986638-44986705 | Common:2; Rare:30 | ||||
| chr7:45768931-45769129 | Common:1; Rare:59 |