| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68903771-68903916 | Common:3; Rare:67; Clinvar (benign):2 | ||||
| chr11:69640790-69641224 | Rare:94 | ||||
| chr11:69641397-69641479 | Rare:23 | ||||
| chr11:70398373-70398614 | Common:2; Rare:88 | ||||
| chr11:71448318-71448614 | Common:3; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452987-71453280 | Common:3; Rare:82 | ||||
| chr11:71928889-71929058 | Common:1; Rare:58 | ||||
| chr11:72080517-72080777 | Common:1; Rare:56; Clinvar:4 | ||||
| chr11:73760267-73760332 | Rare:13 | ||||
| chr11:73787859-73787944 | Common:1; Rare:22 | ||||
| chr11:73876784-73877036 | Common:5; Rare:71 | ||||
| chr11:74170990-74171379 | Common:3; Rare:125 | ||||
| chr11:74949053-74949358 | Common:6; Rare:92 | ||||
| chr11:75562706-75562889 | Common:1; Rare:39 | ||||
| chr11:76783042-76783357 | Common:9; Rare:103 |