| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:151316756-151316922 | Common:1; Rare:30 | ||||
| chr3:152268585-152269358 | Common:2; Rare:261 | ||||
| chr3:152269529-152269749 | Common:2; Rare:64 | ||||
| chr3:152835004-152835128 | Common:1; Rare:46 | ||||
| chr3:154121308-154121444 | Common:2; Rare:62 | ||||
| chr3:155854355-155854772 | Rare:115 | ||||
| chr3:155870355-155870746 | Common:2; Rare:108 | ||||
| chr3:156674364-156674635 | Common:3; Rare:78 | ||||
| chr3:157159833-157159869 | Rare:11 | ||||
| chr3:157160018-157160327 | Rare:128 | ||||
| chr3:157543220-157543416 | Rare:46 | ||||
| chr3:158105739-158105878 | Common:5; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158672560-158672722 | Common:2; Rare:47 | ||||
| chr3:158732131-158732416 | Common:10; Rare:89 | ||||
| chr3:158732744-158732899 | Rare:23 |