Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108746447-108746822 | Common:2; Rare:130 | ||||
chr1:108746862-108747156 | Common:4; Rare:74 | ||||
chr1:108876777-108877217 | Common:2; Rare:119; Clinvar:7; Clinvar (benign):1 | ||||
chr1:108963078-108963611 | Common:5; Rare:176 | ||||
chr1:109042038-109042113 | Rare:18 | ||||
chr1:109075865-109076210 | Common:1; Rare:128 | ||||
chr1:109090557-109090802 | Common:4; Rare:58 | ||||
chr1:109090855-109091225 | Common:1; Rare:105 | ||||
chr1:109213695-109214004 | Rare:113 | ||||
chr1:109214297-109214448 | Rare:28 | ||||
chr1:109283097-109283574 | Common:4; Rare:111 | ||||
chr1:109397863-109398227 | Common:1; Rare:113 | ||||
chr1:109426022-109426207 | Rare:41 | ||||
chr1:109426308-109426891 | Common:4; Rare:190 | ||||
chr1:109483709-109484046 | Common:5; Rare:102 |