| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111879147-111879548 | Common:1; Rare:125 | ||||
| chr11:111912724-111912878 | Rare:32 | ||||
| chr11:111912889-111913102 | Common:3; Rare:48 | ||||
| chr11:111913116-111913314 | Rare:46 | ||||
| chr11:111923484-111923684 | Common:1; Rare:37 | ||||
| chr11:111923728-111923922 | Common:2; Rare:25 | ||||
| chr11:111937135-111937198 | Common:2; Rare:13 | ||||
| chr11:111977097-111977376 | Common:4; Rare:61 | ||||
| chr11:112025026-112025188 | Rare:45; Clinvar:2 | ||||
| chr11:112025339-112025629 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073995-112074373 | Common:1; Rare:80 | ||||
| chr11:112086720-112086921 | Rare:85; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112164032-112164122 | Rare:16 | ||||
| chr11:112226053-112226650 | Common:2; Rare:189; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961372-112961453 | Rare:37 |