Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6473864-6474107 | Rare:78 | ||||
chr11:6481283-6481569 | Common:5; Rare:130 | ||||
chr11:6603536-6603822 | Common:4; Rare:89; Clinvar (benign):3 | ||||
chr11:6604059-6604358 | Common:1; Rare:84; Clinvar (benign):3 | ||||
chr11:6683121-6683160 | Rare:16 | ||||
chr11:6683241-6683656 | Common:6; Rare:158 | ||||
chr11:6926406-6926557 | Common:4; Rare:49 | ||||
chr11:7020312-7020493 | Rare:65 | ||||
chr11:7513617-7514056 | Common:6; Rare:130 | ||||
chr11:7577458-7577569 | Rare:25 | ||||
chr11:7677163-7677384 | Common:2; Rare:39 | ||||
chr11:8682606-8683280 | Common:4; Rare:265 | ||||
chr11:8871359-8871490 | Rare:27 | ||||
chr11:8910942-8911283 | Common:6; Rare:95 | ||||
chr11:8964324-8964569 | Common:4; Rare:92 |