| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69640952-69641357 | Common:1; Rare:98 | ||||
| chr11:69641444-69641511 | Rare:12 | ||||
| chr11:69675309-69675534 | Common:1; Rare:60 | ||||
| chr11:70398439-70398608 | Common:2; Rare:60 | ||||
| chr11:71448305-71448702 | Common:4; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71453023-71453265 | Common:1; Rare:69 | ||||
| chr11:71928652-71929082 | Common:1; Rare:119 | ||||
| chr11:72041534-72041722 | Rare:27 | ||||
| chr11:72080420-72080819 | Common:2; Rare:96; Clinvar:7 | ||||
| chr11:72103193-72103518 | Rare:94 | ||||
| chr11:72112244-72112508 | Rare:66 | ||||
| chr11:72722208-72722546 | Rare:72 | ||||
| chr11:72781672-72782014 | Common:1; Rare:93 | ||||
| chr11:72782318-72782492 | Common:1; Rare:20 | ||||
| chr11:73218159-73218290 | Rare:21 |