Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2556511-2556569 | Rare:19 | ||||
chr1:3690553-3690722 | Common:1; Rare:39 | ||||
chr1:3772478-3772774 | Common:3; Rare:60 | ||||
chr1:3857208-3857517 | Common:1; Rare:77 | ||||
chr1:3900219-3900409 | Common:11; Rare:87 | ||||
chr1:5992400-5992704 | Common:4; Rare:104; Clinvar:6 | ||||
chr1:6199539-6199692 | Rare:55 | ||||
chr1:6206011-6206116 | Common:2; Rare:23 | ||||
chr1:6208680-6208933 | Common:1; Rare:76 | ||||
chr1:6471574-6471761 | Common:1; Rare:63; Clinvar (benign):2 | ||||
chr1:6579803-6580044 | Common:3; Rare:81 | ||||
chr1:6602865-6603116 | Common:3; Rare:88 | ||||
chr1:6603314-6603504 | Common:1; Rare:44 | ||||
chr1:6701790-6701962 | Rare:54 | ||||
chr1:7771132-7771368 | Common:4; Rare:100 |