| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40241326-40242033 | Common:9; Rare:254 | ||||
| chr1:40307480-40307704 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr1:40312465-40312769 | Common:1; Rare:279; Clinvar (benign):14 | ||||
| chr1:40312811-40313211 | Common:4; Rare:68 | ||||
| chr1:40313208-40313358 | Common:2; Rare:27 | ||||
| chr1:40313446-40313846 | Rare:96 | ||||
| chr1:40338647-40339504 | Common:8; Rare:210 | ||||
| chr1:40342258-40342441 | Common:4; Rare:28 | ||||
| chr1:40381105-40381436 | Rare:57 | ||||
| chr1:40381542-40381822 | Common:1; Rare:83 | ||||
| chr1:40383579-40383755 | Rare:34 | ||||
| chr1:40384984-40385190 | Rare:47 | ||||
| chr1:40385602-40386357 | Common:7; Rare:239 | ||||
| chr1:40386736-40387249 | Common:8; Rare:130 | ||||
| chr1:40387435-40387842 | Common:8; Rare:167 |