| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9942727-9942884 | Common:1; Rare:24 | ||||
| chr1:9943291-9943492 | Common:2; Rare:48 | ||||
| chr1:9997126-9997324 | Common:2; Rare:61 | ||||
| chr1:10032795-10033247 | Common:2; Rare:115 | ||||
| chr1:10033322-10033720 | Common:2; Rare:76 | ||||
| chr1:10398829-10399120 | Common:2; Rare:116 | ||||
| chr1:11189162-11189361 | Common:1; Rare:44 | ||||
| chr1:11262493-11262780 | Common:2; Rare:88 | ||||
| chr1:11654384-11654489 | Rare:29 | ||||
| chr1:11654817-11654925 | Common:2; Rare:32 | ||||
| chr1:11805900-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
| chr1:11980081-11980484 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):5 | ||||
| chr1:11981749-11982024 | Common:13; Rare:54; Clinvar (benign):2 | ||||
| chr1:12616364-12616602 | Common:2; Rare:44 | ||||
| chr1:12617207-12617467 | Rare:73 |