| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23868261-23868564 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:23959020-23959235 | Common:3; Rare:39 | ||||
| chr1:23959565-23959855 | Common:5; Rare:75 | ||||
| chr1:23980084-23980525 | Common:2; Rare:110 | ||||
| chr1:23980882-23981039 | Common:2; Rare:31 | ||||
| chr1:24108422-24108581 | Rare:56 | ||||
| chr1:24143067-24143266 | Rare:54 | ||||
| chr1:24187342-24187712 | Common:7; Rare:91 | ||||
| chr1:24413617-24413901 | Common:2; Rare:67 | ||||
| chr1:24415509-24415822 | Common:3; Rare:78 | ||||
| chr1:24502062-24502395 | Common:1; Rare:92 | ||||
| chr1:24503100-24503500 | Common:4; Rare:60 | ||||
| chr1:24555640-24556200 | Common:5; Rare:130 | ||||
| chr1:24642772-24643350 | Common:2; Rare:184 | ||||
| chr1:24745073-24745489 | Common:4; Rare:151 |