Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94459409-94459754 | Rare:87; Clinvar:14; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
chr11:94767650-94767785 | Common:1; Rare:15 | ||||
chr11:96341776-96341902 | Common:1; Rare:37 | ||||
chr11:102398783-102399076 | Common:3; Rare:96 | ||||
chr11:114058753-114058893 | Common:4; Rare:28 | ||||
chr11:114162848-114162898 | Rare:15 | ||||
chr11:114179754-114179828 | Common:1; Rare:7 | ||||
chr11:114886911-114887205 | Rare:43 | ||||
chr11:117290653-117290886 | Common:1; Rare:54 | ||||
chr11:118233417-118233734 | Common:2; Rare:69 | ||||
chr11:118266123-118266217 | Common:1; Rare:16 | ||||
chr11:118791685-118791774 | Common:1; Rare:26 | ||||
chr11:119094661-119094888 | Common:1; Rare:64 | ||||
chr11:120132685-120132782 | Rare:13 | ||||
chr11:126367310-126367384 | Rare:16 |