| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42958821-42959100 | Common:4; Rare:75; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43172077-43172341 | Common:3; Rare:102 | ||||
| chr1:43172560-43172740 | Common:6; Rare:40 | ||||
| chr1:43358662-43359134 | Common:7; Rare:140 | ||||
| chr1:43367946-43368216 | Rare:69 | ||||
| chr1:43389757-43389964 | Common:4; Rare:92 | ||||
| chr1:43649963-43650186 | Rare:57 | ||||
| chr1:43707332-43707604 | Common:2; Rare:84 | ||||
| chr1:43946645-43946987 | Rare:93 | ||||
| chr1:43974811-43975040 | Common:3; Rare:64 | ||||
| chr1:44213382-44213549 | Common:1; Rare:36 | ||||
| chr1:44355270-44355404 | Common:1; Rare:31 | ||||
| chr1:44674421-44674722 | Common:3; Rare:79 | ||||
| chr1:44739627-44739947 | Common:3; Rare:130 | ||||
| chr1:44775435-44775640 | Common:2; Rare:85 |