Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778628-778809 | Common:2; Rare:71 | ||||
chr1:827520-827706 | Common:1; Rare:78 | ||||
chr1:2554027-2554303 | Common:1; Rare:84 | ||||
chr1:9182135-9182240 | Rare:27 | ||||
chr1:9689454-9689602 | Common:1; Rare:37 | ||||
chr1:12618872-12619056 | Rare:34 | ||||
chr1:12619095-12619204 | Rare:23 | ||||
chr1:15800227-15800410 | Rare:33 | ||||
chr1:15834856-15835133 | Common:2; Rare:124 | ||||
chr1:16644653-16644803 | Common:1; Rare:3 | ||||
chr1:16913928-16914100 | Common:7; Rare:33 | ||||
chr1:18926300-18926487 | Rare:36 | ||||
chr1:21827861-21828106 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr1:21857146-21857325 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:25095121-25095252 | Common:1; Rare:16 |