Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:7068037-7068382 | Common:6; Rare:118 | ||||
chr4:10116687-10117089 | Common:8; Rare:190 | ||||
chr4:15681458-15681869 | Common:3; Rare:142 | ||||
chr4:17614555-17614665 | Common:2; Rare:48 | ||||
chr4:17810681-17811043 | Common:4; Rare:113 | ||||
chr4:25160411-25160697 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr4:25914051-25914308 | Common:2; Rare:110 | ||||
chr4:26320917-26321041 | Rare:43 | ||||
chr4:37826514-37826729 | Common:6; Rare:79 | ||||
chr4:37977168-37977459 | Rare:69 | ||||
chr4:39458849-39459122 | Common:3; Rare:155; Clinvar:1; Clinvar (benign):5 | ||||
chr4:39527426-39527746 | Common:2; Rare:80 | ||||
chr4:39638847-39639140 | Common:1; Rare:109 | ||||
chr4:39698007-39698185 | Common:1; Rare:73 | ||||
chr4:41256728-41256994 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2 |