| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:15835793-15836134 | Common:6; Rare:165 | ||||
| chr1:16499211-16499373 | Rare:76 | ||||
| chr1:16514283-16514574 | Common:3; Rare:95 | ||||
| chr1:16535349-16535360 | |||||
| chr1:16644637-16644775 | Common:1; Rare:2 | ||||
| chr1:16765256-16765540 | Common:2; Rare:17 | ||||
| chr1:16889383-16889687 | Common:8; Rare:62 | ||||
| chr1:16895609-16895809 | Common:3; Rare:40 | ||||
| chr1:20650253-20650601 | Common:4; Rare:101; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:20656126-20656316 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr1:21827870-21827984 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:21830051-21830182 | Rare:40 | ||||
| chr1:21831461-21831757 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:21855521-21855913 | Common:4; Rare:132; Clinvar:9; Clinvar (benign):5 | ||||
| chr1:21857014-21857325 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):2 |