Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:134503140-134503645 | Common:6; Rare:137 | ||||
chr5:134506190-134506610 | Common:8; Rare:154 | ||||
chr5:134926602-134927419 | Common:11; Rare:205 | ||||
chr5:135930249-135930375 | Common:3; Rare:52 | ||||
chr5:135973340-135973750 | Common:3; Rare:84 | ||||
chr5:137752930-137753310 | Common:3; Rare:160 | ||||
chr5:138095455-138095753 | Rare:83 | ||||
chr5:138492070-138492193 | Rare:38 | ||||
chr5:138492900-138493370 | Common:2; Rare:110 | ||||
chr5:139026524-139027140 | Common:4; Rare:173; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr5:139504128-139504281 | Rare:31 | ||||
chr5:139517940-139518220 | Common:2; Rare:118 | ||||
chr5:139696704-139697019 | Common:1; Rare:94 | ||||
chr5:139697476-139697664 | Common:2; Rare:58 | ||||
chr5:139699949-139700349 | Common:1; Rare:91 |