Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42929240-42929808 | Common:5; Rare:191 | ||||
chr6:42984284-42984629 | Rare:86 | ||||
chr6:43013875-43014280 | Common:2; Rare:88 | ||||
chr6:43053787-43053987 | Common:1; Rare:65; Clinvar:5 | ||||
chr6:43059804-43059904 | Rare:31 | ||||
chr6:43182084-43182233 | Rare:43 | ||||
chr6:43427481-43427588 | Rare:33 | ||||
chr6:43427774-43427915 | Rare:36 | ||||
chr6:43477493-43477597 | Rare:23 | ||||
chr6:43516846-43517130 | Common:5; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575921-43576234 | Common:2; Rare:125; Clinvar:8 | ||||
chr6:43627297-43627490 | Rare:26 | ||||
chr6:43628811-43628927 | Rare:40 | ||||
chr6:43629097-43629406 | Common:2; Rare:100 | ||||
chr6:43687740-43687841 | Common:1; Rare:44 |