Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114152295-114152575 | Common:1; Rare:68 | ||||
chr1:114152913-114153078 | Common:3; Rare:50 | ||||
chr1:114153628-114154005 | Rare:108 | ||||
chr1:114510927-114511414 | Common:5; Rare:191 | ||||
chr1:114581542-114581848 | Common:1; Rare:134 | ||||
chr1:114669988-114670236 | Common:1; Rare:77 | ||||
chr1:114716659-114716985 | Common:4; Rare:124; Clinvar:5; Clinvar (benign):3 | ||||
chr1:114780394-114780770 | Rare:132 | ||||
chr1:115089413-115089663 | Common:3; Rare:92 | ||||
chr1:115641787-115642027 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116373049-116373398 | Rare:120 | ||||
chr1:116667657-116667966 | Common:3; Rare:100 | ||||
chr1:117060010-117060369 | Common:7; Rare:102 | ||||
chr1:117121394-117121457 | Common:1; Rare:18 | ||||
chr1:117121675-117121981 | Common:1; Rare:97 |