| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:629501-630020 | Common:7; Rare:162 | ||||
| chr1:633651-634154 | Common:14; Rare:357 | ||||
| chr1:778532-778928 | Common:18; Rare:440 | ||||
| chr1:826977-827377 | Common:15; Rare:155 | ||||
| chr1:827417-827829 | Common:10; Rare:424 | ||||
| chr1:904665-905027 | Common:5; Rare:231 | ||||
| chr1:905160-905650 | Common:2; Rare:169 | ||||
| chr1:992400-992710 | Common:2; Rare:46 | ||||
| chr1:998760-999310 | Common:9; Rare:265 | ||||
| chr1:1014412-1014580 | Common:3; Rare:70; Clinvar (benign):2 | ||||
| chr1:1014789-1015527 | Common:12; Rare:231 | ||||
| chr1:1021167-1021698 | Common:5; Rare:172 | ||||
| chr1:1033013-1033548 | Common:2; Rare:217 | ||||
| chr1:1038795-1039041 | Common:18; Rare:108 | ||||
| chr1:1040750-1041280 | Common:9; Rare:133; Clinvar:2; Clinvar (benign):6 |