Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111602160-111602472 | Common:1; Rare:101 | ||||
chr11:111766354-111766442 | Common:1; Rare:51 | ||||
chr11:111878878-111878950 | Common:2; Rare:17 | ||||
chr11:111879146-111879537 | Rare:121 | ||||
chr11:112073987-112074351 | Common:1; Rare:77 | ||||
chr11:112086720-112086928 | Rare:90; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr11:112226304-112226667 | Common:1; Rare:149; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr11:113314454-113314605 | Rare:53 | ||||
chr11:114059421-114059727 | Rare:66 | ||||
chr11:114400455-114400762 | Common:2; Rare:120 | ||||
chr11:116772971-116773107 | Common:1; Rare:45 | ||||
chr11:116787953-116788112 | Rare:47 | ||||
chr11:117144183-117144358 | Common:2; Rare:89 | ||||
chr11:117199018-117199411 | Common:6; Rare:125 | ||||
chr11:117232043-117232163 | Rare:29 |