Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255047-243255358 | Common:1; Rare:69 | ||||
chr1:243255755-243256124 | Rare:104; Clinvar:4 | ||||
chr1:244451686-244451776 | Rare:23 | ||||
chr1:244451814-244452212 | Common:1; Rare:135 | ||||
chr1:244461234-244461325 | Common:1; Rare:26 | ||||
chr1:244835142-244835340 | Rare:81 | ||||
chr1:244835575-244835752 | Common:2; Rare:80; Clinvar (benign):5 | ||||
chr1:244863677-244864609 | Common:1; Rare:311; Clinvar:8; Clinvar (benign):11 | ||||
chr1:244969844-244970163 | Rare:102 | ||||
chr1:244970234-244970418 | Common:4; Rare:90 | ||||
chr1:246566180-246566606 | Common:2; Rare:139 | ||||
chr1:247331603-247331807 | Rare:46 | ||||
chr1:248838086-248838395 | Common:2; Rare:97 | ||||
chr1:248838397-248838441 | Rare:14 | ||||
chr1:248856556-248856702 | Rare:38 |