| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161020741-161020969 | Rare:56 | ||||
| chr1:161021012-161021317 | Common:5; Rare:92 | ||||
| chr1:161041765-161041922 | Rare:42 | ||||
| chr1:161044974-161045088 | Rare:23 | ||||
| chr1:161045860-161046064 | Common:1; Rare:53 | ||||
| chr1:161118012-161118179 | Rare:87 | ||||
| chr1:161131690-161131792 | Rare:18 | ||||
| chr1:161132372-161132700 | Common:1; Rare:102 | ||||
| chr1:161153736-161154093 | Common:1; Rare:109; Clinvar (pathogenic):1 | ||||
| chr1:161166271-161166522 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161199051-161199326 | Rare:43 | ||||
| chr1:161215159-161215383 | Common:2; Rare:79 | ||||
| chr1:161314305-161314412 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:161367857-161367905 | Rare:10 | ||||
| chr1:161505188-161505540 | Common:1; Rare:75 |