Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:22297926-22298196 | Common:13; Rare:108 | ||||
chr22:46052802-46052906 | Rare:21 | ||||
chr3:14125732-14125752 | Rare:2 | ||||
chr3:75435023-75435361 | Common:4; Rare:118 | ||||
chr3:75641108-75641386 | Common:1; Rare:46 | ||||
chr3:101676264-101676474 | Common:2; Rare:69 | ||||
chr3:107240606-107240721 | Rare:47 | ||||
chr3:157174941-157175223 | Common:3; Rare:124 | ||||
chr3:169765053-169765194 | Rare:64; Clinvar (pathogenic):2 | ||||
chr4:30719350-30719663 | Common:1; Rare:71 | ||||
chr4:54232873-54233142 | Common:5; Rare:69 | ||||
chr4:76306570-76306766 | Rare:58 | ||||
chr4:119454600-119454861 | Common:12; Rare:87 | ||||
chr4:143559387-143559494 | Common:1; Rare:32 | ||||
chr4:173509541-173509683 | Common:1; Rare:34 |