Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:44581208-44581462 | Common:2; Rare:57 | ||||
chr7:44800339-44800541 | Common:3; Rare:54 | ||||
chr7:44836628-44836766 | Rare:31 | ||||
chr7:44876422-44876628 | Rare:33 | ||||
chr7:44986536-44986797 | Common:4; Rare:111 | ||||
chr7:45610484-45610740 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr7:45768945-45769158 | Common:2; Rare:68 | ||||
chr7:50880212-50880320 | Rare:15 | ||||
chr7:51869926-51869988 | Rare:10 | ||||
chr7:54146420-54146470 | Rare:8 | ||||
chr7:55646965-55647097 | Rare:26 | ||||
chr7:55997123-55997436 | Common:1; Rare:76 | ||||
chr7:65081260-65081386 | Common:2; Rare:39 | ||||
chr7:65750843-65751115 | Common:3; Rare:121 | ||||
chr7:65751451-65751716 | Common:2; Rare:64 |