| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35088816-35088900 | Rare:19 | ||||
| chr17:35088943-35089163 | Common:2; Rare:53 | ||||
| chr17:35089172-35089614 | Common:7; Rare:104 | ||||
| chr17:35119517-35119723 | Rare:76; Clinvar:18; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr17:35119729-35120059 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:35142064-35142094 | Rare:8 | ||||
| chr17:35142171-35142402 | Common:2; Rare:69 | ||||
| chr17:35242896-35243116 | Rare:76 | ||||
| chr17:35577933-35577988 | Common:1; Rare:19; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:35578330-35578965 | Common:4; Rare:140; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:35586909-35587610 | Common:3; Rare:160 | ||||
| chr17:35587760-35587811 | Rare:7 | ||||
| chr17:35731441-35731713 | Rare:70 | ||||
| chr17:35732053-35732058 | Rare:1 | ||||
| chr17:35808698-35809134 | Common:3; Rare:81 |