Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:35663439-35663680 | Common:3; Rare:43 | ||||
chr18:45865415-45865709 | Rare:73 | ||||
chr18:45866925-45867066 | Rare:37; Clinvar:1 | ||||
chr18:46021583-46021663 | Rare:16 | ||||
chr18:46095090-46095346 | Common:1; Rare:68; Clinvar (benign):1 | ||||
chr18:46815547-46815563 | Rare:1 | ||||
chr18:47885021-47885056 | Rare:7 | ||||
chr18:48568167-48568231 | Common:1; Rare:11 | ||||
chr18:48646282-48646689 | Common:4; Rare:75 | ||||
chr18:48665958-48665995 | Rare:15 | ||||
chr18:48759042-48759206 | Rare:32 | ||||
chr18:55510047-55510225 | Common:1; Rare:32 | ||||
chr18:55573386-55573403 | Rare:2 | ||||
chr18:57630284-57630302 | Rare:4 | ||||
chr18:57630313-57630394 | Rare:20 |