Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241999082-241999145 | Rare:6 | ||||
chr1:243255028-243255433 | Common:1; Rare:99 | ||||
chr1:243255774-243256124 | Rare:100; Clinvar:4 | ||||
chr1:243850663-243850816 | Rare:45 | ||||
chr1:243851056-243851145 | Rare:31 | ||||
chr1:244451649-244452230 | Common:1; Rare:183 | ||||
chr1:244653203-244653274 | Rare:15 | ||||
chr1:244835152-244835430 | Rare:109 | ||||
chr1:244856588-244856885 | Common:1; Rare:63; Clinvar (benign):2 | ||||
chr1:244862891-244863197 | Common:3; Rare:109 | ||||
chr1:244863468-244864407 | Common:2; Rare:313; Clinvar:9; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr1:244864411-244864818 | Common:1; Rare:161 | ||||
chr1:244970026-244970439 | Common:5; Rare:183 | ||||
chr1:246507188-246507359 | Common:1; Rare:67 | ||||
chr1:246566137-246566627 | Common:3; Rare:160 |