| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179954302-179954892 | Common:3; Rare:135 | ||||
| chr1:180154397-180154533 | Common:2; Rare:44 | ||||
| chr1:180154654-180154953 | Common:4; Rare:102 | ||||
| chr1:180502347-180502490 | Rare:40 | ||||
| chr1:180502535-180503076 | Common:1; Rare:201 | ||||
| chr1:180503162-180503425 | Common:2; Rare:59 | ||||
| chr1:180503438-180503452 | Rare:2 | ||||
| chr1:180631821-180632199 | Common:6; Rare:138 | ||||
| chr1:180912913-180913109 | Rare:45 | ||||
| chr1:180913122-180913218 | Rare:25 | ||||
| chr1:181022846-181023289 | Common:26; Rare:197 | ||||
| chr1:181033859-181034020 | Rare:38 | ||||
| chr1:181088447-181088812 | Common:1; Rare:132 | ||||
| chr1:182391064-182391114 | Common:2; Rare:8 | ||||
| chr1:182391639-182392102 | Common:5; Rare:172; Clinvar:6; Clinvar (benign):5 |