Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:5596045-5596142 | Rare:29 | ||||
chr11:5596688-5596812 | Common:2; Rare:41 | ||||
chr11:5624881-5625033 | Rare:25 | ||||
chr11:6234621-6234868 | Common:2; Rare:76 | ||||
chr11:6390225-6390494 | Common:2; Rare:77 | ||||
chr11:6473849-6474102 | Rare:81 | ||||
chr11:6481292-6481556 | Common:5; Rare:120 | ||||
chr11:6603536-6603822 | Common:4; Rare:89; Clinvar (benign):3 | ||||
chr11:6683261-6683507 | Common:5; Rare:112 | ||||
chr11:6926846-6926942 | Common:1; Rare:22 | ||||
chr11:7020301-7020524 | Rare:77 | ||||
chr11:7513625-7513996 | Common:6; Rare:113 | ||||
chr11:7597122-7597219 | Common:2; Rare:16 | ||||
chr11:7673437-7673599 | Common:1; Rare:53 | ||||
chr11:8682644-8682816 | Common:2; Rare:77 |