| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:105610399-105611002 | Common:2; Rare:166 | ||||
| chr11:106022162-106022540 | Common:3; Rare:111 | ||||
| chr11:106077306-106077740 | Common:2; Rare:140 | ||||
| chr11:107457738-107457932 | Common:2; Rare:70 | ||||
| chr11:107565671-107565781 | Rare:30 | ||||
| chr11:107591029-107591392 | Common:3; Rare:114 | ||||
| chr11:107591878-107591909 | Rare:11 | ||||
| chr11:108008832-108009264 | Common:1; Rare:115 | ||||
| chr11:108009273-108009401 | Rare:56 | ||||
| chr11:108121404-108121672 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222549-108223128 | Common:1; Rare:190; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223237-108223441 | Rare:56 | ||||
| chr11:108467522-108467642 | Common:3; Rare:45 | ||||
| chr11:108498010-108498128 | Common:1; Rare:26 | ||||
| chr11:108664839-108665120 | Common:5; Rare:113 |