Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:129567995-129568246 | Rare:43 | ||||
chr9:130459310-130459506 | Common:1; Rare:31 | ||||
chr9:130498923-130499289 | Rare:64 | ||||
chr9:130712992-130713303 | Rare:87 | ||||
chr9:134208634-134208793 | Common:1; Rare:30 | ||||
chr9:134218911-134219097 | Common:1; Rare:29 | ||||
chr9:134220376-134220573 | Rare:45 | ||||
chr9:134372842-134373138 | Common:1; Rare:57 | ||||
chr9:134376800-134377162 | Common:5; Rare:86 | ||||
chr9:136418265-136418669 | Common:4; Rare:114; Clinvar (pathogenic):1 | ||||
chr9:136688091-136688230 | Rare:48 | ||||
chr9:136941627-136941813 | Common:1; Rare:78 | ||||
chrM:15769-16011 | |||||
chrX:2609169-2609436 | Common:1; Rare:86 | ||||
chrX:2934174-2934410 | Common:3; Rare:28 |