| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:630627-630749 | Common:3; Rare:12 | ||||
| chr1:22025046-22025075 | Rare:4 | ||||
| chr1:154972377-154972557 | Rare:26 | ||||
| chr10:80207298-80207443 | Common:1; Rare:30 | ||||
| chr10:87342318-87342432 | Common:2; Rare:38 | ||||
| chr10:100373303-100373632 | Common:3; Rare:70 | ||||
| chr11:65499040-65499152 | Common:1; Rare:97 | ||||
| chr11:65499296-65499724 | Common:1; Rare:219 | ||||
| chr11:65500565-65501164 | Common:2; Rare:287 | ||||
| chr11:65501206-65501245 | Common:2; Rare:20 | ||||
| chr11:65501528-65501567 | Rare:19 | ||||
| chr11:66315065-66315200 | Rare:33 | ||||
| chr12:56642506-56642678 | Rare:46 | ||||
| chr12:76030556-76030628 | Rare:28 | ||||
| chr14:49634311-49634462 | Common:1; Rare:73; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 |