| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:190478386-190478529 | Rare:33 | ||||
| chr1:192808892-192809081 | Common:3; Rare:87 | ||||
| chr1:193059321-193059776 | Common:1; Rare:211 | ||||
| chr1:193105381-193105543 | Common:2; Rare:68 | ||||
| chr1:193121639-193122216 | Common:3; Rare:203; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:193186554-193186654 | Rare:18 | ||||
| chr1:196608868-196609042 | Rare:32 | ||||
| chr1:197146340-197146466 | Rare:59; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr1:197146579-197146794 | Rare:50; Clinvar:3 | ||||
| chr1:197775237-197775494 | Common:1; Rare:65 | ||||
| chr1:197902529-197902644 | Rare:37 | ||||
| chr1:197902913-197902997 | Rare:41 | ||||
| chr1:200409977-200410139 | Rare:54 | ||||
| chr1:200620703-200620930 | Rare:59 | ||||
| chr1:200669829-200670039 | Common:12; Rare:78 |