| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40477178-40477339 | Common:2; Rare:46 | ||||
| chr1:40531487-40531653 | Rare:42 | ||||
| chr1:40691372-40691852 | Common:3; Rare:198 | ||||
| chr1:41242117-41242188 | Rare:18 | ||||
| chr1:42035947-42036174 | Common:1; Rare:58 | ||||
| chr1:42682175-42682424 | Common:2; Rare:63 | ||||
| chr1:42766637-42766938 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:42766972-42767311 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr1:42816938-42817168 | Common:1; Rare:71 | ||||
| chr1:42817185-42817548 | Rare:119 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 | ||||
| chr1:42958744-42959086 | Common:4; Rare:89; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43172087-43172359 | Common:3; Rare:107 | ||||
| chr1:43367958-43368212 | Rare:67 | ||||
| chr1:43389747-43389977 | Common:4; Rare:102; Clinvar:1 |