| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179365649-179365766 | Common:4; Rare:37 | ||||
| chr1:179365894-179366131 | Common:10; Rare:52 | ||||
| chr1:179877740-179877961 | Rare:45 | ||||
| chr1:179881769-179881871 | Rare:26 | ||||
| chr1:179882212-179882349 | Rare:25 | ||||
| chr1:179882418-179883175 | Common:4; Rare:339; Clinvar:11; Clinvar (benign):5 | ||||
| chr1:179883262-179883393 | Common:1; Rare:30 | ||||
| chr1:179954287-179954889 | Common:3; Rare:138 | ||||
| chr1:179955145-179955267 | Common:1; Rare:26 | ||||
| chr1:180154421-180154969 | Common:6; Rare:184 | ||||
| chr1:180502490-180503116 | Common:2; Rare:228 | ||||
| chr1:180631841-180632211 | Common:5; Rare:135 | ||||
| chr1:181022811-181023199 | Common:25; Rare:184 | ||||
| chr1:181033231-181033464 | Common:2; Rare:37 | ||||
| chr1:181033805-181034061 | Rare:60 |