Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231708084-231708348 | Common:1; Rare:108 | ||||
chr2:231708864-231708949 | Common:1; Rare:38 | ||||
chr2:231961643-231961748 | Rare:30; Clinvar:1 | ||||
chr2:232550545-232550723 | Rare:70 | ||||
chr2:232550830-232551078 | Common:1; Rare:58 | ||||
chr2:233854493-233854779 | Common:4; Rare:81 | ||||
chr2:237085748-237085955 | Common:2; Rare:77 | ||||
chr2:237414083-237414392 | Common:2; Rare:61; Clinvar (benign):1 | ||||
chr2:237487136-237487277 | Common:3; Rare:37 | ||||
chr2:237966761-237967077 | Common:4; Rare:96 | ||||
chr2:238060734-238061057 | Common:4; Rare:100 | ||||
chr2:238203616-238203797 | Common:3; Rare:76 | ||||
chr2:238426849-238427067 | Common:1; Rare:84 | ||||
chr2:241102276-241102425 | Common:2; Rare:47 | ||||
chr2:241272770-241272999 | Rare:78 |