Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:95072878-95073023 | Rare:54 | ||||
chr1:95233955-95234227 | Common:5; Rare:81 | ||||
chr1:99969922-99970039 | Rare:32 | ||||
chr1:100037973-100038125 | Common:1; Rare:62 | ||||
chr1:100132928-100133194 | Common:2; Rare:92 | ||||
chr1:100249809-100250017 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266114-100266313 | Common:2; Rare:73 | ||||
chr1:100894802-100894889 | Rare:16 | ||||
chr1:100895975-100896155 | Rare:49 | ||||
chr1:101025763-101025920 | Common:1; Rare:48 | ||||
chr1:101236611-101236928 | Common:2; Rare:58 | ||||
chr1:108200129-108200414 | Common:7; Rare:88 | ||||
chr1:108963436-108963592 | Rare:54 | ||||
chr1:109090673-109090835 | Common:3; Rare:33 | ||||
chr1:109426367-109426645 | Common:2; Rare:100 |