Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:61971234-61971489 | Rare:41 | ||||
chr2:65204812-65204985 | Rare:30 | ||||
chr2:68872560-68872730 | Rare:34 | ||||
chr2:68872753-68872835 | Rare:22 | ||||
chr2:68872844-68873076 | Rare:49 | ||||
chr2:68873109-68873161 | Rare:13 | ||||
chr2:68873229-68873269 | Rare:3 | ||||
chr2:68911482-68911563 | Rare:16 | ||||
chr2:70086267-70086372 | Common:2; Rare:45 | ||||
chr2:71716973-71717306 | Common:1; Rare:77 | ||||
chr2:74120093-74120385 | Common:1; Rare:98 | ||||
chr2:74120568-74120650 | Common:1; Rare:23 | ||||
chr2:74370474-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
chr2:74377431-74377734 | Common:1; Rare:77 | ||||
chr2:88016545-88016822 | Common:8; Rare:116 |