Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119366779-119367034 | Common:1; Rare:74 | ||||
chr2:119759784-119759801 | Rare:5 | ||||
chr2:121530574-121530884 | Common:7; Rare:131 | ||||
chr2:121649418-121649645 | Common:2; Rare:65 | ||||
chr2:121736766-121737229 | Common:5; Rare:184 | ||||
chr2:121755359-121755716 | Common:3; Rare:113 | ||||
chr2:127294079-127294246 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387973-127388184 | Common:2; Rare:89 | ||||
chr2:127811139-127811320 | Common:1; Rare:61 | ||||
chr2:127858112-127858219 | Common:1; Rare:51 | ||||
chr2:127885884-127885972 | Rare:19 | ||||
chr2:128091064-128091354 | Common:8; Rare:94 | ||||
chr2:130181553-130181696 | Common:1; Rare:48 | ||||
chr2:130342118-130342218 | Rare:43; Clinvar:1 | ||||
chr2:130342645-130342929 | Common:5; Rare:89 |