Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217089587-217089785 | Rare:45 | ||||
chr1:217089902-217089944 | Rare:7 | ||||
chr1:217630963-217631379 | Common:3; Rare:121 | ||||
chr1:218285213-218285409 | Common:2; Rare:88 | ||||
chr1:218346405-218346753 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):6 | ||||
chr1:219173771-219173902 | Common:1; Rare:70 | ||||
chr1:220272333-220272548 | Rare:64; Clinvar:5 | ||||
chr1:221742056-221742288 | Rare:60 | ||||
chr1:222589866-222589940 | Common:2; Rare:21 | ||||
chr1:222644159-222644387 | Common:1; Rare:65 | ||||
chr1:222712437-222712872 | Common:3; Rare:151 | ||||
chr1:223143240-223143368 | Common:3; Rare:35 | ||||
chr1:224113976-224114135 | Common:1; Rare:58 | ||||
chr1:224183020-224183289 | Common:3; Rare:111 | ||||
chr1:224330126-224330439 | Common:6; Rare:95 |