| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44405096-44405308 | Rare:46 | ||||
| chr1:44405759-44405940 | Common:1; Rare:45 | ||||
| chr1:44408761-44408924 | Common:1; Rare:28 | ||||
| chr1:44412974-44413478 | Common:3; Rare:179 | ||||
| chr1:44631880-44631999 | Common:3; Rare:37 | ||||
| chr1:44632305-44632501 | Common:3; Rare:95 | ||||
| chr1:44674091-44674374 | Common:1; Rare:90 | ||||
| chr1:44674413-44674759 | Common:3; Rare:92 | ||||
| chr1:44739610-44739881 | Common:2; Rare:103 | ||||
| chr1:44775230-44775620 | Common:2; Rare:122 | ||||
| chr1:44775674-44775926 | Common:3; Rare:86 | ||||
| chr1:44799780-44800042 | Common:3; Rare:47 | ||||
| chr1:44800050-44800420 | Common:2; Rare:92 | ||||
| chr1:44843242-44843472 | Rare:59 | ||||
| chr1:44986506-44986774 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):1 |