| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:180503379-180503499 | Rare:26 | ||||
| chr1:180631816-180632199 | Common:6; Rare:140 | ||||
| chr1:180632253-180632267 | Rare:2 | ||||
| chr1:180632419-180632499 | Rare:23 | ||||
| chr1:181022483-181022637 | Common:3; Rare:50 | ||||
| chr1:181022677-181023291 | Common:26; Rare:272 | ||||
| chr1:181033186-181033229 | Rare:5 | ||||
| chr1:181033245-181033500 | Common:2; Rare:42 | ||||
| chr1:181033602-181033711 | Common:2; Rare:18 | ||||
| chr1:181033816-181034027 | Rare:51 | ||||
| chr1:181034098-181034195 | Rare:25 | ||||
| chr1:181034210-181034305 | Common:1; Rare:12 | ||||
| chr1:181088435-181089013 | Common:2; Rare:210 | ||||
| chr1:181089066-181089239 | Common:3; Rare:61 | ||||
| chr1:182390511-182390756 | Common:1; Rare:61; Clinvar:6; Clinvar (benign):1 |