Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:133308829-133308990 | Rare:75 | ||||
chr10:133347120-133347414 | Rare:61 | ||||
chr11:207361-207719 | Common:7; Rare:110 | ||||
chr11:208688-208857 | Rare:69 | ||||
chr11:236720-237059 | Common:4; Rare:108 | ||||
chr11:289707-289942 | Common:1; Rare:66 | ||||
chr11:290162-290460 | Common:2; Rare:101 | ||||
chr11:307579-307792 | Common:6; Rare:61 | ||||
chr11:320703-321054 | Common:12; Rare:102; Clinvar:1 | ||||
chr11:506608-507001 | Common:3; Rare:120 | ||||
chr11:507122-507290 | Rare:58 | ||||
chr11:535418-535679 | Common:5; Rare:110; Clinvar (benign):1 | ||||
chr11:560710-561003 | Common:5; Rare:137 | ||||
chr11:576412-576531 | Rare:48 | ||||
chr11:615946-616033 | Common:1; Rare:27 |