Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:102346950-102347293 | Common:7; Rare:92 | ||||
chr11:102452659-102452878 | Rare:69 | ||||
chr11:103092057-103092259 | Common:1; Rare:66 | ||||
chr11:106077317-106077706 | Common:2; Rare:117 | ||||
chr11:107457787-107457940 | Common:1; Rare:51 | ||||
chr11:108009295-108009349 | Rare:29 | ||||
chr11:108121429-108121634 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):5 | ||||
chr11:108222594-108222956 | Rare:120; Clinvar:3 | ||||
chr11:110296560-110296788 | Rare:120; Clinvar:6 | ||||
chr11:111602222-111602497 | Common:1; Rare:92 | ||||
chr11:111766327-111766459 | Common:1; Rare:85 | ||||
chr11:111879152-111879554 | Common:1; Rare:122 | ||||
chr11:112073995-112074351 | Common:1; Rare:73 | ||||
chr11:112086710-112086905 | Rare:82; Clinvar:1 | ||||
chr11:112226249-112226435 | Rare:73 |