Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:53348912-53349253 | Common:2; Rare:114 | ||||
chr6:56542875-56543118 | Common:1; Rare:36 | ||||
chr6:56843639-56843932 | Common:9; Rare:65 | ||||
chr6:57089894-57090200 | Rare:108 | ||||
chr6:57172207-57172348 | Rare:41 | ||||
chr6:73262923-73263279 | Common:4; Rare:94 | ||||
chr6:73461439-73461839 | Common:2; Rare:95; Clinvar (benign):1 | ||||
chr6:73696070-73696217 | Rare:26 | ||||
chr6:73696224-73696278 | Rare:29 | ||||
chr6:73696281-73696356 | Common:1; Rare:30 | ||||
chr6:75284742-75285000 | Common:1; Rare:70 | ||||
chr6:79537394-79537543 | Common:1; Rare:36; Clinvar:2 | ||||
chr6:83193222-83193395 | Common:3; Rare:62 | ||||
chr6:85449524-85449769 | Common:2; Rare:63 | ||||
chr6:85449957-85450317 | Common:1; Rare:104 |