| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1206591-1207340 | Common:9; Rare:322 | ||||
| chr1:1212730-1213274 | Common:4; Rare:245; Clinvar (benign):4 | ||||
| chr1:1214106-1214315 | Rare:91 | ||||
| chr1:1231866-1232320 | Rare:411; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr1:1232350-1232620 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:1273690-1274127 | Common:8; Rare:465 | ||||
| chr1:1305200-1305540 | Common:1; Rare:84 | ||||
| chr1:1305640-1305864 | Common:1; Rare:141 | ||||
| chr1:1307838-1308664 | Common:34; Rare:821 | ||||
| chr1:1324533-1324949 | Common:14; Rare:627 | ||||
| chr1:1325020-1325930 | Common:10; Rare:324 | ||||
| chr1:1330738-1331138 | Common:5; Rare:133 | ||||
| chr1:1348602-1349218 | Common:4; Rare:415 | ||||
| chr1:1349278-1349703 | Common:6; Rare:334 | ||||
| chr1:1375108-1375665 | Common:27; Rare:545 |