Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:169704357-169704405 | Common:2; Rare:7 | ||||
chr7:21898457-21898743 | Common:2; Rare:74 | ||||
chr7:25025249-25025388 | Rare:23 | ||||
chr7:26193251-26193694 | Rare:155; Clinvar (benign):2 | ||||
chr7:26198067-26198285 | Common:1; Rare:79 | ||||
chr7:26198859-26198905 | Rare:14 | ||||
chr7:27118222-27118277 | Rare:18 | ||||
chr7:27118308-27118443 | Common:1; Rare:25 | ||||
chr7:30569829-30570097 | Rare:51 | ||||
chr7:32942344-32942347 | Rare:1 | ||||
chr7:38335574-38335866 | Common:2; Rare:64 | ||||
chr7:44467578-44467843 | Common:2; Rare:42 | ||||
chr7:44876447-44876769 | Rare:53 | ||||
chr7:45768895-45769063 | Common:2; Rare:45 | ||||
chr7:55463637-55463878 | Common:1; Rare:39 |