Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111720633-111720913 | Common:1; Rare:62 | ||||
chr11:111745988-111746038 | Rare:7 | ||||
chr11:111837508-111837746 | Common:1; Rare:59; Clinvar (benign):3 | ||||
chr11:114154535-114154875 | Common:1; Rare:52 | ||||
chr11:114155197-114155350 | Common:1; Rare:29 | ||||
chr11:114179643-114179834 | Common:1; Rare:27 | ||||
chr11:114198144-114198433 | Common:1; Rare:54 | ||||
chr11:114258397-114258692 | Common:1; Rare:50 | ||||
chr11:114291783-114292091 | Common:1; Rare:51 | ||||
chr11:114313403-114313665 | Common:1; Rare:56 | ||||
chr11:118406744-118406965 | Common:2; Rare:52 | ||||
chr11:118608505-118608830 | Rare:71 | ||||
chr11:118622432-118622498 | Rare:10 | ||||
chr11:118791693-118791763 | Rare:18 | ||||
chr11:118909276-118909415 | Common:1; Rare:33 |