Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:76949611-76949864 | Common:1; Rare:72 | ||||
chr4:77075945-77076058 | Rare:70 | ||||
chr4:77862621-77862904 | Common:3; Rare:108 | ||||
chr4:78939368-78939541 | Common:1; Rare:88 | ||||
chr4:82373758-82374046 | Rare:83 | ||||
chr4:82374118-82374144 | Rare:10 | ||||
chr4:82429247-82429642 | Common:2; Rare:213; Clinvar:13; Clinvar (benign):8 | ||||
chr4:82430462-82430843 | Common:2; Rare:131 | ||||
chr4:82900528-82900735 | Rare:59 | ||||
chr4:83455808-83456080 | Common:2; Rare:106 | ||||
chr4:84966651-84966777 | Rare:33 | ||||
chr4:86934714-86935067 | Common:2; Rare:119 | ||||
chr4:88007503-88007675 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
chr4:88284530-88284944 | Common:2; Rare:101 | ||||
chr4:88378981-88379082 | Rare:34 |