Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125691450-125691578 | Rare:42 | ||||
chr11:9758177-9758366 | Rare:54 | ||||
chr11:12989521-12989614 | Common:2; Rare:24 | ||||
chr11:19714554-19714756 | Common:1; Rare:37 | ||||
chr11:19714766-19714782 | Rare:4 | ||||
chr11:22624608-22624781 | Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr11:57778552-57778834 | Rare:51 | ||||
chr11:65421134-65421466 | Rare:70 | ||||
chr11:65422657-65422805 | Common:2; Rare:44 | ||||
chr11:67805312-67805514 | Common:2; Rare:74 | ||||
chr11:70935143-70935252 | Common:1; Rare:23 | ||||
chr11:75492303-75492405 | Common:1; Rare:21 | ||||
chr11:96341773-96341902 | Common:1; Rare:37 | ||||
chr11:117290653-117290722 | Common:1; Rare:19 | ||||
chr11:118909407-118909459 | Rare:13 |