| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124092342-124092550 | Common:1; Rare:51 | ||||
| chr10:124093488-124093631 | Common:1; Rare:26 | ||||
| chr10:124418905-124419112 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:124791736-124791938 | Common:1; Rare:105 | ||||
| chr10:124801751-124801860 | Rare:43 | ||||
| chr10:125719416-125719802 | Common:1; Rare:149 | ||||
| chr10:125823112-125823573 | Common:2; Rare:158; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:129466957-129467285 | Common:5; Rare:134; Clinvar:1 | ||||
| chr10:130136215-130136465 | Common:7; Rare:107 | ||||
| chr10:132186709-132186942 | Common:10; Rare:62 | ||||
| chr10:132331784-132332166 | Common:17; Rare:126 | ||||
| chr10:133308828-133308989 | Rare:75 | ||||
| chr10:133326240-133326341 | Rare:28 | ||||
| chr10:133393987-133394337 | Common:2; Rare:149 | ||||
| chr11:207372-207726 | Common:7; Rare:104 |