Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:141923726-141923902 | Common:1; Rare:49 | ||||
chr5:149141397-149141508 | Rare:31 | ||||
chr5:149551375-149551635 | Rare:61 | ||||
chr5:150758997-150759093 | Common:2; Rare:41 | ||||
chr5:151080958-151081154 | Common:1; Rare:66 | ||||
chr5:154941038-154941137 | Rare:49 | ||||
chr5:157859000-157859255 | Common:2; Rare:78 | ||||
chr5:163437297-163437607 | Rare:87 | ||||
chr5:168486328-168486491 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr5:171387518-171387888 | Rare:166 | ||||
chr5:172771191-172771433 | Common:4; Rare:103 | ||||
chr5:173328394-173328602 | Rare:41 | ||||
chr5:176388575-176388811 | Common:4; Rare:90 | ||||
chr5:177022586-177022732 | Common:1; Rare:53 | ||||
chr6:693092-693221 | Rare:35 |