| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1231928-1232361 | Rare:161; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr1:1273799-1274083 | Common:2; Rare:106 | ||||
| chr1:1324620-1324778 | Common:1; Rare:83 | ||||
| chr1:1358526-1358865 | Common:2; Rare:110 | ||||
| chr1:1399307-1399597 | Common:1; Rare:128 | ||||
| chr1:1407229-1407365 | Common:1; Rare:57 | ||||
| chr1:1435610-1435751 | Rare:52 | ||||
| chr1:1658952-1659035 | Common:1; Rare:30 | ||||
| chr1:1724286-1724496 | Common:4; Rare:75 | ||||
| chr1:2391550-2391951 | Common:2; Rare:139 | ||||
| chr1:2586445-2586523 | Rare:18 | ||||
| chr1:3624751-3625052 | Common:1; Rare:101 | ||||
| chr1:3857161-3857511 | Common:2; Rare:100 | ||||
| chr1:3900219-3900415 | Common:11; Rare:87 | ||||
| chr1:5992411-5992753 | Common:4; Rare:110; Clinvar:4 |