| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923944-95924164 | Common:1; Rare:96; Clinvar (benign):2 | ||||
| chr11:96389846-96390061 | Common:1; Rare:93 | ||||
| chr11:101583468-101583561 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:101914828-101915033 | Common:2; Rare:51 | ||||
| chr11:101915124-101915369 | Common:3; Rare:75 | ||||
| chr11:102317201-102317499 | Rare:50 | ||||
| chr11:102347129-102347298 | Common:2; Rare:60 | ||||
| chr11:102452612-102452943 | Common:2; Rare:103 | ||||
| chr11:104163990-104164186 | Common:1; Rare:50 | ||||
| chr11:106077335-106077690 | Common:2; Rare:103 | ||||
| chr11:108009273-108009366 | Rare:42 | ||||
| chr11:108222580-108222964 | Rare:126; Clinvar:3 | ||||
| chr11:108353595-108353819 | Common:1; Rare:35; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:110296574-110296788 | Rare:113; Clinvar:5 | ||||
| chr11:111541471-111541558 | Common:1; Rare:19 |