Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:25376993-25377325 | Common:3; Rare:100 | ||||
chr4:25914051-25914316 | Common:2; Rare:114 | ||||
chr4:26320903-26321046 | Rare:52; Clinvar (benign):1 | ||||
chr4:26583966-26584122 | Rare:31 | ||||
chr4:37826418-37826729 | Common:8; Rare:102 | ||||
chr4:37977189-37977459 | Rare:66 | ||||
chr4:38867617-38867826 | Common:2; Rare:78 | ||||
chr4:39182328-39182548 | Rare:48; Clinvar:2 | ||||
chr4:39366324-39366394 | Rare:22 | ||||
chr4:39458839-39459109 | Common:3; Rare:151; Clinvar (benign):5 | ||||
chr4:39527354-39527754 | Common:3; Rare:97 | ||||
chr4:39638838-39639140 | Common:1; Rare:112 | ||||
chr4:39697911-39698188 | Common:2; Rare:117 | ||||
chr4:41256748-41257001 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr4:41990372-41990580 | Common:1; Rare:75 |