Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:208615-208847 | Rare:82 | ||||
chr11:236324-236522 | Common:6; Rare:65 | ||||
chr11:289008-289138 | Rare:38 | ||||
chr11:320554-321012 | Common:10; Rare:158; Clinvar:1 | ||||
chr11:504845-505141 | Common:4; Rare:74 | ||||
chr11:506737-507001 | Common:3; Rare:90 | ||||
chr11:560718-561003 | Common:5; Rare:129 | ||||
chr11:576412-576591 | Rare:74 | ||||
chr11:615946-616033 | Common:1; Rare:27 | ||||
chr11:695731-695817 | Rare:29 | ||||
chr11:721069-721341 | Rare:116 | ||||
chr11:747290-747565 | Rare:119; Clinvar:5; Clinvar (benign):1 | ||||
chr11:777460-777578 | Common:1; Rare:53 | ||||
chr11:809498-809575 | Rare:22 | ||||
chr11:809780-810038 | Common:2; Rare:115 |