| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40508662-40508799 | Common:4; Rare:37 | ||||
| chr1:40531514-40531696 | Rare:45 | ||||
| chr1:40691448-40691860 | Common:3; Rare:179 | ||||
| chr1:40692045-40692224 | Common:1; Rare:58 | ||||
| chr1:40979520-40979766 | Common:3; Rare:89 | ||||
| chr1:41242104-41242358 | Rare:74 | ||||
| chr1:42335134-42335280 | Common:2; Rare:67 | ||||
| chr1:42335855-42336143 | Rare:56 | ||||
| chr1:42455980-42456583 | Common:1; Rare:184 | ||||
| chr1:42658271-42658463 | Common:2; Rare:56 | ||||
| chr1:42682158-42682432 | Common:2; Rare:70 | ||||
| chr1:42767023-42767309 | Common:4; Rare:88 | ||||
| chr1:42816986-42817136 | Common:1; Rare:39 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 | ||||
| chr1:42958857-42959063 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):2 |