| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44986532-44986652 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr1:44986720-44986812 | Rare:19 | ||||
| chr1:45010903-45011194 | Common:2; Rare:83 | ||||
| chr1:45011917-45012285 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45012625-45013004 | Common:1; Rare:103 | ||||
| chr1:45339938-45340044 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr1:45340109-45340232 | Rare:54; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:45340381-45340480 | Common:1; Rare:26; Clinvar:1 | ||||
| chr1:45500046-45500386 | Common:1; Rare:95; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521699-45522089 | Common:1; Rare:138 | ||||
| chr1:45550730-45551105 | Common:3; Rare:91 | ||||
| chr1:45583801-45584170 | Common:1; Rare:131 | ||||
| chr1:45687050-45687353 | Common:1; Rare:81 | ||||
| chr1:45688055-45688273 | Common:1; Rare:60 | ||||
| chr1:45750617-45750800 | Rare:68 |