Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:56435481-56435741 | Common:5; Rare:97 | ||||
chr4:56467542-56467662 | Common:2; Rare:51; Clinvar (benign):4 | ||||
chr4:56977551-56977741 | Common:2; Rare:73 | ||||
chr4:67701124-67701358 | Common:4; Rare:109 | ||||
chr4:68349952-68350209 | Common:1; Rare:95 | ||||
chr4:70993492-70993627 | Common:3; Rare:35 | ||||
chr4:73998464-73998494 | Rare:16 | ||||
chr4:74158045-74158135 | Rare:37 | ||||
chr4:75514268-75514482 | Common:1; Rare:71 | ||||
chr4:75673344-75673648 | Common:1; Rare:125 | ||||
chr4:75724375-75724721 | Common:1; Rare:95 | ||||
chr4:76147838-76147957 | Common:2; Rare:31 | ||||
chr4:76148366-76148579 | Common:3; Rare:67 | ||||
chr4:76949559-76949859 | Common:1; Rare:94 | ||||
chr4:77075971-77076105 | Common:3; Rare:66 |