Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:24426410-24426776 | Common:5; Rare:135 | ||||
chr18:25351056-25351387 | Common:2; Rare:75 | ||||
chr18:25352019-25352588 | Common:2; Rare:186 | ||||
chr18:26090503-26090896 | Common:4; Rare:155 | ||||
chr18:26226209-26226487 | Common:5; Rare:99 | ||||
chr18:26546639-26546883 | Common:1; Rare:49 | ||||
chr18:26657374-26657453 | Rare:23 | ||||
chr18:27185250-27185453 | Common:3; Rare:74 | ||||
chr18:28177013-28177320 | Common:3; Rare:150 | ||||
chr18:31102050-31102493 | Common:1; Rare:104; Clinvar:9 | ||||
chr18:31497894-31498262 | Common:1; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
chr18:31685429-31685524 | Rare:39 | ||||
chr18:31943033-31943386 | Common:7; Rare:112 | ||||
chr18:32018404-32018758 | Common:2; Rare:101 | ||||
chr18:32091561-32091990 | Common:10; Rare:111 |