Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86396008-86396074 | Common:1; Rare:21 | ||||
chr1:86396261-86396410 | Common:2; Rare:37 | ||||
chr1:86704719-86704882 | Common:2; Rare:62 | ||||
chr1:86914339-86914823 | Common:1; Rare:152 | ||||
chr1:87329101-87329173 | Common:1; Rare:17 | ||||
chr1:88683960-88684359 | Common:4; Rare:117 | ||||
chr1:88891485-88891677 | Common:1; Rare:90 | ||||
chr1:89994977-89995174 | Common:2; Rare:75 | ||||
chr1:91021963-91022418 | Common:1; Rare:112 | ||||
chr1:91500568-91500910 | Common:3; Rare:85 | ||||
chr1:92298929-92299079 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
chr1:92785062-92785368 | Common:6; Rare:101 | ||||
chr1:92961436-92961799 | Common:3; Rare:106 | ||||
chr1:93079064-93079298 | Common:3; Rare:100 | ||||
chr1:93180067-93180083 | Rare:6 |