| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119205770-119206075 | Common:3; Rare:157 | ||||
| chr11:119206175-119206386 | Common:10; Rare:184; Clinvar:15; Clinvar (benign):8 | ||||
| chr11:119317111-119317275 | Rare:111 | ||||
| chr11:119318354-119318504 | Common:2; Rare:26 | ||||
| chr11:119318630-119319110 | Common:2; Rare:112 | ||||
| chr11:119334252-119334603 | Rare:176 | ||||
| chr11:119381547-119381847 | Common:2; Rare:160 | ||||
| chr11:120185050-120185390 | Common:5; Rare:118 | ||||
| chr11:120185400-120185800 | Common:4; Rare:104 | ||||
| chr11:120210460-120211209 | Common:17; Rare:284 | ||||
| chr11:120336087-120336591 | Rare:323 | ||||
| chr11:121292563-121292821 | Rare:86; Clinvar:3 | ||||
| chr11:121451220-121451800 | Common:2; Rare:165 | ||||
| chr11:121452045-121452451 | Common:2; Rare:180 | ||||
| chr11:123062071-123062363 | Common:5; Rare:224 |