Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119679090-119679212 | Common:3; Rare:40 | ||||
chr2:120252582-120252961 | Common:3; Rare:124 | ||||
chr2:121530589-121530880 | Common:7; Rare:115 | ||||
chr2:121736745-121737231 | Common:5; Rare:197 | ||||
chr2:127294111-127294219 | Common:2; Rare:41; Clinvar (benign):2 | ||||
chr2:127387958-127388283 | Common:7; Rare:142 | ||||
chr2:127811145-127811259 | Rare:35 | ||||
chr2:128091054-128091355 | Common:8; Rare:98 | ||||
chr2:130181528-130181668 | Common:2; Rare:54 | ||||
chr2:130182072-130182330 | Common:2; Rare:100 | ||||
chr2:130342127-130342279 | Rare:60 | ||||
chr2:131093382-131093533 | Common:1; Rare:70 | ||||
chr2:131105194-131105362 | Common:1; Rare:74 | ||||
chr2:134918702-134918852 | Rare:59 | ||||
chr2:135531172-135531508 | Common:1; Rare:70 |