Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:23308534-23308818 | Common:2; Rare:57 | ||||
chr7:23351723-23351796 | Common:2; Rare:24 | ||||
chr7:23465464-23465490 | Rare:9 | ||||
chr7:26193008-26193725 | Common:1; Rare:261; Clinvar (benign):2 | ||||
chr7:26197814-26198045 | Common:3; Rare:94 | ||||
chr7:26198062-26198417 | Common:3; Rare:136 | ||||
chr7:26199177-26199347 | Rare:62 | ||||
chr7:27121950-27121961 | Rare:2 | ||||
chr7:27122323-27122573 | Common:1; Rare:47 | ||||
chr7:27641934-27642125 | Common:2; Rare:34 | ||||
chr7:28037270-28037557 | Common:1; Rare:39 | ||||
chr7:29684915-29684991 | Rare:25 | ||||
chr7:29685037-29685146 | Common:3; Rare:39 | ||||
chr7:29988070-29988162 | Rare:15 | ||||
chr7:30460402-30460512 | Rare:30 |