| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:201021784-201022007 | Rare:40 | ||||
| chr1:201025443-201025843 | Common:2; Rare:83 | ||||
| chr1:201053230-201053580 | Common:3; Rare:110; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr1:201170610-201171043 | Common:4; Rare:200 | ||||
| chr1:201391660-201392040 | Rare:124 | ||||
| chr1:201392250-201392708 | Common:2; Rare:106 | ||||
| chr1:201405470-201405626 | Common:2; Rare:30 | ||||
| chr1:201420366-201420637 | Common:4; Rare:103 | ||||
| chr1:201453990-201454390 | Common:7; Rare:146 | ||||
| chr1:201456717-201457117 | Common:1; Rare:75 | ||||
| chr1:201467418-201467818 | Common:16; Rare:128 | ||||
| chr1:201476619-201477019 | Rare:141 | ||||
| chr1:201480418-201480670 | Common:1; Rare:74 | ||||
| chr1:201480710-201480940 | Common:6; Rare:55 | ||||
| chr1:201482177-201482387 | Common:3; Rare:62 |