Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:83077341-83077603 | Common:1; Rare:76 | ||||
chr5:134004662-134004838 | Common:1; Rare:69 | ||||
chr5:140647609-140647848 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691305-140691497 | Common:1; Rare:73; Clinvar:8 | ||||
chr5:141320759-141320886 | Common:1; Rare:35 | ||||
chr5:149551367-149551622 | Rare:59 | ||||
chr5:157731336-157731438 | Common:4; Rare:33 | ||||
chr5:172006613-172006950 | Common:1; Rare:74 | ||||
chr5:177022631-177022741 | Rare:42 | ||||
chr6:13615168-13615405 | Common:2; Rare:108 | ||||
chr6:24666905-24667248 | Common:3; Rare:128 | ||||
chr6:30067049-30067237 | Common:2; Rare:33 | ||||
chr6:30557229-30557361 | Common:1; Rare:50 | ||||
chr6:30571213-30571482 | Common:1; Rare:87 | ||||
chr6:31665867-31666101 | Common:3; Rare:63 |