Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:87521334-87521511 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr6:87543026-87543196 | Common:2; Rare:28 | ||||
chr6:89333180-89333223 | Common:1; Rare:8 | ||||
chr6:89338518-89338584 | Rare:17 | ||||
chr6:99565130-99565257 | Rare:19 | ||||
chr6:100505895-100505951 | Rare:13 | ||||
chr6:100606791-100607014 | Common:1; Rare:69 | ||||
chr6:101464676-101464920 | Rare:48 | ||||
chr6:101763523-101763603 | Common:1; Rare:8 | ||||
chr6:105281517-105281810 | Common:2; Rare:57 | ||||
chr6:108678310-108678456 | Rare:23 | ||||
chr6:108879529-108879744 | Common:2; Rare:42 | ||||
chr6:109454004-109454438 | Common:2; Rare:109 | ||||
chr6:111307283-111307396 | Common:1; Rare:32 | ||||
chr6:113953082-113953375 | Rare:59 |