Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:13726246-13726309 | Rare:15 | ||||
chr18:13726388-13726720 | Common:4; Rare:122 | ||||
chr18:21111127-21111289 | Rare:32 | ||||
chr18:21111783-21111971 | Common:2; Rare:54 | ||||
chr18:21600644-21600800 | Rare:40 | ||||
chr18:21612204-21612441 | Common:1; Rare:70 | ||||
chr18:22169314-22169640 | Common:2; Rare:86 | ||||
chr18:22933256-22933385 | Common:1; Rare:46; Clinvar (benign):1 | ||||
chr18:23453085-23453353 | Rare:94 | ||||
chr18:23503300-23503542 | Common:2; Rare:86 | ||||
chr18:23586396-23586550 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24271777-24272077 | Rare:65 | ||||
chr18:24397774-24398102 | Common:2; Rare:117 | ||||
chr18:24426620-24426765 | Common:3; Rare:61 | ||||
chr18:25350952-25351129 | Rare:62 |