| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:10976193-10976248 | Rare:15 | ||||
| chr1:11012189-11012767 | Common:4; Rare:156; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:11012983-11013269 | Common:1; Rare:100 | ||||
| chr1:11058646-11058740 | Rare:26 | ||||
| chr1:11058880-11059139 | Common:3; Rare:57 | ||||
| chr1:11059291-11059349 | Rare:6 | ||||
| chr1:11059484-11059704 | Common:1; Rare:55 | ||||
| chr1:11059764-11060487 | Common:4; Rare:226 | ||||
| chr1:11099339-11099481 | Rare:35 | ||||
| chr1:11099601-11100057 | Common:4; Rare:173 | ||||
| chr1:11262060-11262192 | Common:2; Rare:29 | ||||
| chr1:11262434-11262952 | Common:3; Rare:147 | ||||
| chr1:11272851-11273372 | Common:2; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:11273391-11273550 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:11273598-11274021 | Common:1; Rare:131; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 |