Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94541684-94541986 | Common:1; Rare:88 | ||||
chr1:94820264-94820419 | Common:2; Rare:45 | ||||
chr1:94926953-94927017 | Common:1; Rare:14 | ||||
chr1:95072857-95073017 | Common:1; Rare:66; Clinvar (benign):2 | ||||
chr1:95233955-95234231 | Common:5; Rare:82 | ||||
chr1:98661553-98661869 | Common:3; Rare:114 | ||||
chr1:99969943-99970062 | Rare:32 | ||||
chr1:100037983-100038138 | Common:1; Rare:62 | ||||
chr1:100132915-100133214 | Common:2; Rare:109 | ||||
chr1:100266107-100266313 | Common:3; Rare:77 | ||||
chr1:100894658-100894914 | Common:1; Rare:62 | ||||
chr1:100895987-100896155 | Rare:46 | ||||
chr1:101025763-101025920 | Common:1; Rare:48 | ||||
chr1:101236611-101236921 | Common:2; Rare:55 | ||||
chr1:103525483-103525723 | Rare:64 |