Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:160419021-160419206 | Common:3; Rare:75 | ||||
chr5:161546637-161547086 | Common:1; Rare:88; Clinvar (benign):3 | ||||
chr5:161547100-161547597 | Common:1; Rare:74 | ||||
chr5:161547613-161547881 | Rare:70 | ||||
chr5:161548038-161548153 | Rare:29; Clinvar (benign):4 | ||||
chr5:161548158-161548238 | Rare:17 | ||||
chr5:161847939-161848276 | Rare:57; Clinvar:2; Clinvar (benign):5 | ||||
chr5:161848486-161848593 | Common:2; Rare:33 | ||||
chr5:161850606-161850808 | Rare:45; Clinvar (benign):4 | ||||
chr5:162067380-162068068 | Common:2; Rare:175; Clinvar:8; Clinvar (benign):4 | ||||
chr5:163437297-163437659 | Rare:108 | ||||
chr5:163459736-163459841 | Rare:26 | ||||
chr5:163459951-163460181 | Common:2; Rare:93 | ||||
chr5:163460344-163460660 | Common:5; Rare:69 | ||||
chr5:163505475-163505669 | Rare:67 |