Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16206498-16206806 | Common:7; Rare:78 | ||||
chr1:16206977-16207196 | Rare:77 | ||||
chr1:16237152-16237353 | Rare:62 | ||||
chr1:16352361-16352622 | Common:3; Rare:136 | ||||
chr1:16366951-16367298 | Common:1; Rare:111 | ||||
chr1:16367469-16367626 | Common:3; Rare:49 | ||||
chr1:16430666-16430898 | Rare:28 | ||||
chr1:16440518-16440778 | Common:2; Rare:76 | ||||
chr1:16613460-16613713 | Common:3; Rare:1 | ||||
chr1:16921807-16921942 | Rare:21 | ||||
chr1:16979940-16980420 | Common:12; Rare:72 | ||||
chr1:17011923-17012136 | Common:2; Rare:59 | ||||
chr1:17053969-17054375 | Common:3; Rare:126; Clinvar:15; Clinvar (benign):10 | ||||
chr1:17439627-17439997 | Rare:121 | ||||
chr1:18902757-18903040 | Common:7; Rare:63 |