Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119102447-119102620 | Common:1; Rare:32 | ||||
chr11:119107263-119107486 | Common:1; Rare:58 | ||||
chr11:119121191-119121624 | Common:1; Rare:108 | ||||
chr11:119168970-119169190 | Rare:49 | ||||
chr11:119205806-119206077 | Common:2; Rare:82 | ||||
chr11:119206201-119206386 | Common:4; Rare:83; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119206639-119207162 | Common:3; Rare:174 | ||||
chr11:119317108-119317317 | Rare:68 | ||||
chr11:119321051-119321560 | Common:7; Rare:245 | ||||
chr11:119334213-119334570 | Rare:97 | ||||
chr11:119375610-119375889 | Common:2; Rare:50 | ||||
chr11:119376249-119376475 | Common:1; Rare:51 | ||||
chr11:119381560-119381860 | Common:1; Rare:79 | ||||
chr11:119421851-119422267 | Common:1; Rare:130 | ||||
chr11:119423167-119423387 | Common:3; Rare:48 |