| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36992801-36992930 | Rare:41 | ||||
| chr3:36992966-36993596 | Common:2; Rare:211; Clinvar:37; Clinvar (benign):17; Clinvar (pathogenic):4 | ||||
| chr3:36993717-36993917 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:37175501-37175612 | Common:1; Rare:23 | ||||
| chr3:37176237-37176675 | Common:1; Rare:130 | ||||
| chr3:37243077-37243529 | Common:4; Rare:127 | ||||
| chr3:37243583-37243670 | Common:1; Rare:43 | ||||
| chr3:37994079-37994565 | Rare:160 | ||||
| chr3:37998936-37999192 | Common:4; Rare:83 | ||||
| chr3:38024530-38024685 | Common:1; Rare:54 | ||||
| chr3:38136007-38136157 | Common:1; Rare:31 | ||||
| chr3:38136374-38136664 | Rare:78 | ||||
| chr3:38136981-38137529 | Common:1; Rare:149 | ||||
| chr3:38138504-38138777 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38138886-38138955 | Rare:24 |