| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160449495-160449621 | Rare:22 | ||||
| chr3:160449710-160450080 | Common:2; Rare:128 | ||||
| chr3:160565535-160565842 | Common:2; Rare:108 | ||||
| chr3:160755429-160755664 | Common:1; Rare:85 | ||||
| chr3:161105243-161105389 | Common:2; Rare:52 | ||||
| chr3:161221151-161221388 | Common:2; Rare:79 | ||||
| chr3:161372842-161373003 | Common:1; Rare:31 | ||||
| chr3:167734813-167735233 | Common:3; Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735611-167735754 | Rare:36 | ||||
| chr3:168095377-168095441 | Rare:15 | ||||
| chr3:168095868-168096260 | Common:1; Rare:126 | ||||
| chr3:169772687-169772825 | Common:1; Rare:35 | ||||
| chr3:169773313-169773424 | Rare:37 | ||||
| chr3:169812480-169812595 | Common:1; Rare:34 | ||||
| chr3:169812875-169813053 | Common:2; Rare:30 |