| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823200-125823594 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896466-125896585 | Rare:4 | ||||
| chr10:126905255-126905489 | Rare:93 | ||||
| chr10:127986910-127987353 | Common:3; Rare:86 | ||||
| chr10:131981861-131982154 | Common:4; Rare:110 | ||||
| chr10:132331784-132332193 | Common:17; Rare:132 | ||||
| chr10:133308821-133309003 | Rare:87 | ||||
| chr10:133565543-133565830 | Common:5; Rare:98 | ||||
| chr11:207343-207740 | Common:9; Rare:137 | ||||
| chr11:208615-208873 | Rare:95 | ||||
| chr11:236331-236559 | Common:8; Rare:74 | ||||
| chr11:307579-307792 | Common:6; Rare:61 | ||||
| chr11:308078-308437 | Common:8; Rare:121 | ||||
| chr11:506732-506976 | Common:3; Rare:85 | ||||
| chr11:560710-561003 | Common:5; Rare:137 |