Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:39527266-39527449 | Common:4; Rare:46 | ||||
chr4:39527502-39527746 | Common:2; Rare:61 | ||||
chr4:39527941-39528043 | Rare:26 | ||||
chr4:39638823-39639173 | Common:1; Rare:127 | ||||
chr4:41261564-41261725 | Common:1; Rare:31; Clinvar (benign):1 | ||||
chr4:41612876-41613005 | Common:1; Rare:20 | ||||
chr4:41990410-41990590 | Common:1; Rare:66 | ||||
chr4:52659173-52659428 | Common:1; Rare:85 | ||||
chr4:55395863-55395987 | Rare:36; Clinvar:2 | ||||
chr4:55853492-55853810 | Rare:91 | ||||
chr4:56387397-56387545 | Rare:53 | ||||
chr4:56435464-56435774 | Common:5; Rare:111 | ||||
chr4:56467542-56467708 | Common:2; Rare:68; Clinvar (benign):5 | ||||
chr4:56977513-56977787 | Common:2; Rare:100 | ||||
chr4:57009554-57009598 | Common:1; Rare:5 |