| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231422267-231422700 | Common:6; Rare:182; Clinvar:9; Clinvar (benign):6 | ||||
| chr1:232599806-232600006 | Common:1; Rare:35 | ||||
| chr1:232953015-232953072 | Rare:13 | ||||
| chr1:232965743-232965890 | Common:1; Rare:28 | ||||
| chr1:233459541-233459626 | Rare:15 | ||||
| chr1:233599124-233599404 | Common:3; Rare:39 | ||||
| chr1:233599863-233599950 | Common:1; Rare:14 | ||||
| chr1:233615050-233615179 | Common:1; Rare:21 | ||||
| chr1:233673514-233673716 | Common:2; Rare:32 | ||||
| chr1:233673874-233673982 | Rare:21 | ||||
| chr1:233676006-233676136 | Common:2; Rare:27 | ||||
| chr1:234356387-234356710 | Common:3; Rare:62 | ||||
| chr1:234356836-234357048 | Common:3; Rare:68 | ||||
| chr1:234398966-234399266 | Common:2; Rare:47 | ||||
| chr1:234495361-234495412 | Rare:7 |