Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:37493815-37494121 | Common:3; Rare:54 | ||||
chr8:127794357-127794575 | Rare:56 | ||||
chr9:35684248-35684503 | Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
chr9:62802625-62802781 | |||||
chr9:111366282-111366528 | Common:2; Rare:57 | ||||
chr9:136438947-136439097 | Rare:54 | ||||
chr9:136728178-136728352 | Common:3; Rare:68 | ||||
chrM:260-843 | |||||
chrM:1388-1833 | |||||
chrM:1841-2120 | |||||
chrM:3872-3954 | |||||
chrM:13272-13422 | |||||
chrM:15381-15895 | |||||
chrX:15675609-15675714 | Rare:18 |