Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86704710-86704966 | Common:3; Rare:92 | ||||
chr1:86914302-86914827 | Common:2; Rare:158 | ||||
chr1:87328290-87328466 | Common:2; Rare:50 | ||||
chr1:88684103-88684359 | Common:2; Rare:67 | ||||
chr1:88684465-88684601 | Common:1; Rare:36 | ||||
chr1:89065203-89065472 | Common:2; Rare:40 | ||||
chr1:89843326-89843487 | Common:1; Rare:66 | ||||
chr1:89994981-89995218 | Common:2; Rare:89 | ||||
chr1:91021954-91022320 | Rare:98 | ||||
chr1:91500666-91500901 | Common:2; Rare:72 | ||||
chr1:91886099-91886325 | Rare:93 | ||||
chr1:92298944-92299094 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92784983-92785243 | Common:4; Rare:102 | ||||
chr1:92831874-92832112 | Common:1; Rare:107; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961436-92961623 | Rare:68 |