Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89994981-89995184 | Common:2; Rare:75 | ||||
chr1:91021978-91022338 | Rare:95 | ||||
chr1:91886068-91886318 | Rare:102 | ||||
chr1:92298945-92299071 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92831808-92832113 | Common:1; Rare:127; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92833137-92833458 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
chr1:93179766-93179922 | Common:1; Rare:28 | ||||
chr1:93180052-93180270 | Rare:80 | ||||
chr1:93180298-93180769 | Common:2; Rare:191 | ||||
chr1:93345766-93345965 | Common:4; Rare:80 | ||||
chr1:93879083-93879279 | Common:1; Rare:75 | ||||
chr1:94820217-94820410 | Common:2; Rare:57 | ||||
chr1:94903132-94903445 | Common:1; Rare:63 | ||||
chr1:94926842-94926957 | Rare:34 | ||||
chr1:94926961-94927157 | Common:3; Rare:63 |