Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:506128-506561 | Common:4; Rare:101 | ||||
chr11:534708-534956 | Common:2; Rare:75 | ||||
chr11:535234-535482 | Common:4; Rare:87; Clinvar (benign):2 | ||||
chr11:535489-535832 | Common:6; Rare:130 | ||||
chr11:537295-537566 | Common:5; Rare:90 | ||||
chr11:560606-561068 | Common:8; Rare:211 | ||||
chr11:561104-561214 | Rare:36 | ||||
chr11:561507-561568 | Rare:19 | ||||
chr11:561590-561629 | Rare:12 | ||||
chr11:575790-576320 | Common:6; Rare:124 | ||||
chr11:576363-576621 | Rare:95 | ||||
chr11:576704-576915 | Common:3; Rare:35 | ||||
chr11:614804-614832 | Rare:9 | ||||
chr11:615020-615213 | Common:1; Rare:88 | ||||
chr11:615881-616146 | Common:2; Rare:86 |