Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51519230-51519487 | Common:9; Rare:96 | ||||
chr1:51729666-51729890 | Common:2; Rare:63 | ||||
chr1:51878333-51878532 | Common:1; Rare:68 | ||||
chr1:52056066-52056335 | Common:2; Rare:74 | ||||
chr1:52404456-52404747 | Common:2; Rare:92 | ||||
chr1:52553066-52553367 | Common:4; Rare:86 | ||||
chr1:52553443-52553674 | Common:2; Rare:67 | ||||
chr1:53196668-53196863 | Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
chr1:53220547-53220688 | Common:1; Rare:71 | ||||
chr1:53238460-53238598 | Rare:61 | ||||
chr1:53889749-53889835 | Rare:33 | ||||
chr1:53946282-53946453 | Rare:63 | ||||
chr1:54053190-54053713 | Common:6; Rare:166 | ||||
chr1:54199990-54200196 | Rare:41 | ||||
chr1:55215346-55215423 | Rare:37 |