| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119178792-119178935 | Common:3; Rare:55 | ||||
| chr10:119892528-119892744 | Common:2; Rare:73 | ||||
| chr10:124418900-124419092 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:125719462-125719734 | Common:1; Rare:86 | ||||
| chr10:125823200-125823560 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:133308835-133309003 | Rare:78 | ||||
| chr11:207361-207511 | Common:4; Rare:60 | ||||
| chr11:208727-208843 | Rare:48 | ||||
| chr11:236839-237044 | Common:2; Rare:75 | ||||
| chr11:777465-777598 | Common:1; Rare:58 | ||||
| chr11:832855-833014 | Common:7; Rare:58 | ||||
| chr11:842494-842984 | Common:8; Rare:197 | ||||
| chr11:4094558-4094870 | Common:2; Rare:86 | ||||
| chr11:5624866-5625029 | Rare:31 | ||||
| chr11:5689672-5689886 | Common:1; Rare:46 |