Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6473871-6474124 | Rare:80 | ||||
chr11:6481292-6481524 | Common:4; Rare:92 | ||||
chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:6683290-6683455 | Common:4; Rare:79 | ||||
chr11:7020316-7020462 | Rare:48 | ||||
chr11:8682623-8682799 | Common:2; Rare:76 | ||||
chr11:8910935-8911252 | Common:6; Rare:88 | ||||
chr11:8964348-8964492 | Common:3; Rare:59 | ||||
chr11:9003996-9004151 | Common:1; Rare:56 | ||||
chr11:9314550-9314769 | Common:1; Rare:76 | ||||
chr11:9663895-9664139 | Common:3; Rare:71 | ||||
chr11:10304907-10305088 | Common:1; Rare:40 | ||||
chr11:10541145-10541293 | Rare:52 | ||||
chr11:10751113-10751289 | Rare:54 | ||||
chr11:10808817-10809220 | Common:4; Rare:169 |