Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86914316-86914746 | Common:1; Rare:127 | ||||
chr1:88684070-88684345 | Common:3; Rare:74 | ||||
chr1:88891495-88891708 | Common:1; Rare:98 | ||||
chr1:89022788-89022958 | Rare:23 | ||||
chr1:89065195-89065443 | Common:1; Rare:37 | ||||
chr1:89198917-89199002 | Rare:9 | ||||
chr1:89994981-89995165 | Common:2; Rare:74 | ||||
chr1:91021963-91022182 | Rare:66 | ||||
chr1:91500718-91500901 | Common:2; Rare:60 | ||||
chr1:91886148-91886334 | Rare:80 | ||||
chr1:92298945-92299071 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92785149-92785464 | Common:6; Rare:85 | ||||
chr1:92831874-92832116 | Common:1; Rare:108; Clinvar:7; Clinvar (benign):5 | ||||
chr1:92961430-92961581 | Rare:59 | ||||
chr1:93079125-93079303 | Common:2; Rare:73 |