| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383582-39383683 | Rare:24; Clinvar:1 | ||||
| chr3:39406582-39406763 | Common:2; Rare:77 | ||||
| chr3:40309431-40309964 | Common:9; Rare:177 | ||||
| chr3:40457212-40457368 | Common:2; Rare:76 | ||||
| chr3:40477087-40477184 | Common:1; Rare:27 | ||||
| chr3:40524815-40525007 | Common:1; Rare:55 | ||||
| chr3:42581904-42582206 | Common:3; Rare:89 | ||||
| chr3:42590744-42590903 | Common:2; Rare:49 | ||||
| chr3:42600351-42600761 | Common:3; Rare:160 | ||||
| chr3:42600867-42601010 | Rare:53 | ||||
| chr3:42773206-42773351 | Common:1; Rare:42 | ||||
| chr3:42804422-42804684 | Common:2; Rare:84 | ||||
| chr3:42936306-42936422 | Common:1; Rare:34 | ||||
| chr3:43286431-43286654 | Common:2; Rare:97 | ||||
| chr3:43690562-43690986 | Common:5; Rare:165; Clinvar:7; Clinvar (benign):2 |