Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:88385242-88385394 | Rare:15 | ||||
chr14:88385497-88385695 | Common:2; Rare:51 | ||||
chr14:88551462-88551630 | Common:3; Rare:41 | ||||
chr14:88562844-88563131 | Rare:131 | ||||
chr14:88563422-88563580 | Rare:67 | ||||
chr14:88824335-88824708 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
chr14:89351474-89351681 | Common:1; Rare:49 | ||||
chr14:89417055-89417345 | Rare:75 | ||||
chr14:89618953-89619346 | Common:1; Rare:125 | ||||
chr14:89619479-89619547 | Rare:16 | ||||
chr14:89954434-89954978 | Common:3; Rare:174 | ||||
chr14:89955693-89956010 | Common:10; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
chr14:89956376-89956633 | Common:5; Rare:63; Clinvar (benign):4 | ||||
chr14:90256424-90256632 | Common:3; Rare:68 | ||||
chr14:90331581-90331779 | Common:1; Rare:50 |