| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:162722913-162723008 | Common:4; Rare:21 | ||||
| chr3:165885563-165885850 | Common:5; Rare:61 | ||||
| chr3:167422752-167422755 | Rare:1 | ||||
| chr3:167430808-167431092 | Common:2; Rare:59 | ||||
| chr3:167433650-167433873 | Common:6; Rare:60 | ||||
| chr3:167671442-167671692 | Rare:44 | ||||
| chr3:168249564-168249693 | Common:1; Rare:35 | ||||
| chr3:168518821-168518976 | Rare:28 | ||||
| chr3:168782341-168782575 | Common:1; Rare:50 | ||||
| chr3:169765001-169765191 | Common:1; Rare:86; Clinvar:7; Clinvar (pathogenic):3 | ||||
| chr3:169769205-169769316 | Common:1; Rare:20 | ||||
| chr3:169769321-169769349 | Rare:11 | ||||
| chr3:170356745-170357008 | Common:2; Rare:109 | ||||
| chr3:170685837-170685839 | |||||
| chr3:171458052-171458254 | Rare:41 |