| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:167935919-167936281 | Common:2; Rare:208 | ||||
| chr1:167936508-167936995 | Common:2; Rare:321 | ||||
| chr1:167937433-167937833 | Common:2; Rare:139 | ||||
| chr1:168178689-168179056 | Common:8; Rare:210 | ||||
| chr1:168179110-168179560 | Rare:200 | ||||
| chr1:168225886-168226103 | Common:4; Rare:136 | ||||
| chr1:169105605-169106005 | Common:4; Rare:113 | ||||
| chr1:169106140-169106453 | Common:6; Rare:221 | ||||
| chr1:169367727-169368268 | Common:6; Rare:227 | ||||
| chr1:169485692-169486224 | Common:2; Rare:213; Clinvar:7; Clinvar (benign):4 | ||||
| chr1:169794510-169794790 | Common:2; Rare:71 | ||||
| chr1:169794855-169795126 | Common:6; Rare:115 | ||||
| chr1:169893492-169893892 | Common:5; Rare:173 | ||||
| chr1:169893857-169894033 | Common:3; Rare:78 | ||||
| chr1:169894190-169894470 | Common:6; Rare:150 |