Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121285200-121285321 | Rare:37 | ||||
chr2:121530583-121530884 | Common:7; Rare:124 | ||||
chr2:121649418-121649645 | Common:2; Rare:65 | ||||
chr2:121736828-121737220 | Common:5; Rare:148 | ||||
chr2:127294091-127294219 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387931-127388255 | Common:9; Rare:139 | ||||
chr2:127526435-127526598 | Common:2; Rare:51 | ||||
chr2:127645996-127646037 | Rare:8 | ||||
chr2:127811118-127811258 | Rare:46 | ||||
chr2:127885900-127885972 | Rare:16 | ||||
chr2:128091039-128091335 | Common:8; Rare:99 | ||||
chr2:130181571-130181775 | Common:2; Rare:89 | ||||
chr2:130182101-130182318 | Common:2; Rare:81 | ||||
chr2:130182438-130182569 | Common:1; Rare:50 | ||||
chr2:130342123-130342232 | Rare:45; Clinvar:1 |