| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823192-125823573 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:131981760-131981990 | Common:4; Rare:80 | ||||
| chr10:132331817-132332193 | Common:13; Rare:114 | ||||
| chr10:133308829-133308989 | Rare:75 | ||||
| chr11:207340-207526 | Common:5; Rare:86 | ||||
| chr11:208661-208860 | Rare:78 | ||||
| chr11:236331-236522 | Common:6; Rare:58 | ||||
| chr11:236919-237039 | Common:1; Rare:46 | ||||
| chr11:288988-289128 | Rare:37 | ||||
| chr11:307579-307791 | Common:6; Rare:61 | ||||
| chr11:320716-321029 | Common:11; Rare:96; Clinvar:1 | ||||
| chr11:407089-407396 | Common:7; Rare:97 | ||||
| chr11:506747-506986 | Common:2; Rare:78 | ||||
| chr11:560710-561003 | Common:5; Rare:137 | ||||
| chr11:576428-576531 | Rare:40 |