Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119678960-119679224 | Common:5; Rare:73 | ||||
chr2:119760046-119760247 | Common:1; Rare:45 | ||||
chr2:120252603-120252967 | Common:3; Rare:120 | ||||
chr2:121285167-121285340 | Common:2; Rare:65 | ||||
chr2:121530568-121530889 | Common:7; Rare:136; Clinvar (pathogenic):1 | ||||
chr2:121649415-121649702 | Common:2; Rare:82 | ||||
chr2:121649928-121650133 | Rare:58 | ||||
chr2:121736744-121737249 | Common:5; Rare:206 | ||||
chr2:126655824-126656275 | Common:1; Rare:121 | ||||
chr2:127294077-127294235 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387949-127388255 | Common:7; Rare:131 | ||||
chr2:127526418-127526596 | Common:2; Rare:60 | ||||
chr2:127811121-127811248 | Rare:41 | ||||
chr2:127858112-127858211 | Rare:48 | ||||
chr2:127885877-127885974 | Rare:20 |