Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:14304411-14304633 | Common:2; Rare:41 | ||||
chr1:15649593-15649806 | Rare:50 | ||||
chr1:15721179-15721383 | Common:1; Rare:42 | ||||
chr1:15834895-15835133 | Common:1; Rare:105 | ||||
chr1:15835805-15836139 | Common:6; Rare:162 | ||||
chr1:16131761-16132161 | Common:1; Rare:110; Clinvar (benign):3 | ||||
chr1:16155002-16155275 | Common:1; Rare:56 | ||||
chr1:16158994-16159102 | Rare:24 | ||||
chr1:16185001-16185190 | Common:2; Rare:29 | ||||
chr1:16217318-16217676 | Common:1; Rare:57 | ||||
chr1:16499217-16499367 | Rare:69 | ||||
chr1:16644645-16644790 | Common:1; Rare:2 | ||||
chr1:16889624-16889687 | Common:2; Rare:15 | ||||
chr1:16895622-16895809 | Common:2; Rare:35 | ||||
chr1:16904815-16904995 | Common:2; Rare:22 |