Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155127650-155128076 | Common:4; Rare:248 | ||||
chr1:155135090-155135517 | Common:1; Rare:388 | ||||
chr1:155135600-155136050 | Common:26; Rare:900 | ||||
chr1:155136091-155136499 | Common:12; Rare:367 | ||||
chr1:155137207-155138032 | Common:1; Rare:396 | ||||
chr1:155139530-155140770 | Common:16; Rare:748; Clinvar:16; Clinvar (benign):32; Clinvar (pathogenic):6 | ||||
chr1:155172439-155172839 | Rare:162 | ||||
chr1:155173120-155173520 | Common:18; Rare:712 | ||||
chr1:155192860-155193822 | Common:6; Rare:736 | ||||
chr1:155207061-155208164 | Common:9; Rare:524 | ||||
chr1:155208487-155208978 | Rare:548 | ||||
chr1:155208900-155209610 | Common:2; Rare:778 | ||||
chr1:155241095-155241495 | Common:2; Rare:115; Clinvar:2 | ||||
chr1:155241619-155242019 | Rare:72 | ||||
chr1:155244471-155245030 | Common:16; Rare:585 |