Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:180802792-180802976 | Common:8; Rare:74 | ||||
chr5:180810126-180810219 | Rare:20 | ||||
chr5:181223118-181223299 | Rare:60 | ||||
chr5:181261060-181261262 | Rare:68 | ||||
chr6:2971542-2971870 | Common:1; Rare:86 | ||||
chr6:2999558-2999893 | Common:11; Rare:72 | ||||
chr6:3118513-3118735 | Common:3; Rare:71 | ||||
chr6:5260720-5261013 | Common:2; Rare:92; Clinvar (benign):2 | ||||
chr6:5261280-5261534 | Common:9; Rare:56 | ||||
chr6:7313095-7313380 | Common:5; Rare:108 | ||||
chr6:7389758-7389820 | Rare:15 | ||||
chr6:7541385-7541643 | Rare:83; Clinvar (benign):1 | ||||
chr6:8435361-8435654 | Common:4; Rare:104 | ||||
chr6:10694630-10694981 | Common:4; Rare:86 | ||||
chr6:10747493-10747881 | Common:4; Rare:134 |