Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31865313-31865581 | Rare:75 | ||||
chr6:31865688-31865920 | Common:1; Rare:65 | ||||
chr6:31874720-31875019 | Common:2; Rare:96 | ||||
chr6:31887885-31888073 | Common:1; Rare:56 | ||||
chr6:32853249-32853411 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr6:32894554-32894803 | Common:9; Rare:68 | ||||
chr6:32980453-32980712 | Common:8; Rare:120 | ||||
chr6:33677359-33677565 | Rare:50 | ||||
chr6:33686828-33687065 | Rare:40 | ||||
chr6:34958906-34959047 | Rare:27 | ||||
chr6:35392250-35392466 | Common:2; Rare:32 | ||||
chr6:35490099-35490402 | Common:1; Rare:87 | ||||
chr6:35602761-35602805 | Rare:13 | ||||
chr6:35609759-35610115 | Common:1; Rare:64 | ||||
chr6:35664902-35665293 | Common:3; Rare:54 |