| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823200-125823594 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896258-125896628 | Common:5; Rare:31 | ||||
| chr10:126905275-126905458 | Rare:70 | ||||
| chr10:131981897-131982158 | Common:1; Rare:96 | ||||
| chr10:132331813-132332155 | Common:14; Rare:108 | ||||
| chr10:133308835-133308989 | Rare:72 | ||||
| chr11:207338-207737 | Common:8; Rare:137 | ||||
| chr11:208688-208873 | Rare:76 | ||||
| chr11:236333-236513 | Common:6; Rare:52 | ||||
| chr11:236857-237044 | Common:2; Rare:72 | ||||
| chr11:506728-506994 | Common:3; Rare:89 | ||||
| chr11:560710-561003 | Common:5; Rare:137 | ||||
| chr11:777461-777642 | Common:2; Rare:81 | ||||
| chr11:809536-809655 | Common:2; Rare:30 | ||||
| chr11:832826-833020 | Common:7; Rare:64 |