| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11934486-11934754 | Common:5; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:11979926-11980328 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:16440617-16440753 | Rare:43 | ||||
| chr1:16613486-16613671 | Common:2 | ||||
| chr1:19210254-19210417 | Rare:63 | ||||
| chr1:19251512-19251838 | Common:6; Rare:106 | ||||
| chr1:21290421-21290439 | Rare:4 | ||||
| chr1:21345467-21345670 | Common:2; Rare:77 | ||||
| chr1:23369795-23369938 | Rare:25 | ||||
| chr1:23424623-23424882 | Common:1; Rare:78 | ||||
| chr1:23559479-23559643 | Common:1; Rare:68 | ||||
| chr1:23691726-23691826 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:23778275-23778523 | Common:9; Rare:124 | ||||
| chr1:23825421-23825537 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:23868259-23868445 | Common:5; Rare:61; Clinvar:1; Clinvar (benign):4 |