| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:155644377-155644725 | Common:2; Rare:121 | ||||
| chr7:156640541-156640756 | Common:3; Rare:105 | ||||
| chr7:156949582-156949743 | Common:2; Rare:50 | ||||
| chr7:157336744-157337091 | Common:5; Rare:166; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704715-158704983 | Common:1; Rare:91 | ||||
| chr8:232210-232377 | Common:2; Rare:65 | ||||
| chr8:406887-406999 | Rare:40 | ||||
| chr8:731154-731412 | Common:3; Rare:96 | ||||
| chr8:6406518-6406673 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708194-6708373 | Common:3; Rare:70 | ||||
| chr8:8386414-8386748 | Common:3; Rare:117 | ||||
| chr8:9151537-9151781 | Common:2; Rare:86 | ||||
| chr8:9555665-9555936 | Common:6; Rare:104 | ||||
| chr8:10839820-10840116 | Common:3; Rare:96 | ||||
| chr8:11201812-11201857 | Rare:10 |