Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:125111712-125111990 | Common:3; Rare:57 | ||||
chr11:125592451-125592884 | Common:6; Rare:148 | ||||
chr11:125625852-125625982 | Rare:43 | ||||
chr11:125887513-125887730 | Common:2; Rare:62 | ||||
chr11:126211613-126211806 | Rare:90 | ||||
chr11:126268814-126269209 | Common:2; Rare:153; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126270490-126270499 | |||||
chr11:126303984-126304112 | Rare:77 | ||||
chr11:128522248-128522525 | Common:1; Rare:83 | ||||
chr11:128693803-128694224 | Common:2; Rare:79 | ||||
chr11:128757912-128758235 | Rare:76 | ||||
chr11:130002819-130002973 | Common:1; Rare:31 | ||||
chr11:130314395-130314528 | Common:1; Rare:46 | ||||
chr11:134253290-134253576 | Common:2; Rare:99; Clinvar (benign):1 | ||||
chr12:389248-389360 | Rare:39 |