Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:81801321-81801510 | Rare:67 | ||||
chr1:85582209-85582621 | Common:1; Rare:123 | ||||
chr1:90851567-90851762 | Common:2; Rare:52 | ||||
chr1:91569920-91570071 | Rare:27 | ||||
chr1:91795650-91795978 | Common:1; Rare:53 | ||||
chr1:92833321-92833624 | Rare:84; Clinvar (pathogenic):1 | ||||
chr1:92840555-92840719 | Rare:46; Clinvar:1 | ||||
chr1:94532394-94532786 | Rare:73 | ||||
chr1:94539685-94539714 | Rare:2 | ||||
chr1:94679707-94679958 | Common:3; Rare:49 | ||||
chr1:95625196-95625559 | Common:2; Rare:53 | ||||
chr1:96722420-96722656 | Common:2; Rare:61 | ||||
chr1:108050271-108050439 | Common:2; Rare:29 | ||||
chr1:109100037-109100334 | Common:3; Rare:138 | ||||
chr1:109100342-109100385 | Rare:15 |