| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124093483-124093812 | Common:2; Rare:62 | ||||
| chr10:124418875-124419092 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:124461766-124461886 | Common:3; Rare:51 | ||||
| chr10:124791756-124791964 | Common:1; Rare:107 | ||||
| chr10:125719449-125719752 | Common:1; Rare:106 | ||||
| chr10:125823200-125823616 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896282-125896639 | Common:5; Rare:32 | ||||
| chr10:126905290-126905473 | Rare:70 | ||||
| chr10:127906940-127907245 | Common:3; Rare:83 | ||||
| chr10:130136327-130136489 | Common:7; Rare:66 | ||||
| chr10:131981760-131982139 | Common:4; Rare:130 | ||||
| chr10:132331786-132332182 | Common:17; Rare:130 | ||||
| chr10:132942558-132942677 | Common:2; Rare:32 | ||||
| chr10:133308829-133309032 | Common:1; Rare:92 | ||||
| chr10:133565507-133565815 | Common:3; Rare:115 |