Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:11611546-11611795 | Common:1; Rare:167 | ||||
chr10:11823258-11823420 | Common:2; Rare:55 | ||||
chr10:12042717-12042991 | Rare:71 | ||||
chr10:12043100-12043460 | Common:4; Rare:200 | ||||
chr10:12068697-12069119 | Common:5; Rare:282 | ||||
chr10:12129388-12129730 | Rare:230 | ||||
chr10:12195767-12196316 | Rare:286 | ||||
chr10:12349352-12349678 | Common:3; Rare:127 | ||||
chr10:13099949-13100205 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13161289-13161611 | Common:2; Rare:164 | ||||
chr10:13299490-13299770 | Common:6; Rare:96 | ||||
chr10:13300051-13300194 | Rare:93; Clinvar:2 | ||||
chr10:13301910-13302260 | Common:3; Rare:98 | ||||
chr10:13347640-13347850 | Common:3; Rare:85 | ||||
chr10:13347952-13348443 | Rare:238 |