Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16895618-16895809 | Common:2; Rare:36 | ||||
chr1:16913905-16914115 | Common:7; Rare:43 | ||||
chr1:19255281-19255284 | |||||
chr1:19255300-19255328 | Common:1; Rare:3 | ||||
chr1:19255339-19255460 | Common:2; Rare:25 | ||||
chr1:19258357-19258514 | Rare:33 | ||||
chr1:19267182-19267244 | Rare:9 | ||||
chr1:19273399-19273477 | Common:3; Rare:14 | ||||
chr1:19273958-19274261 | Common:5; Rare:95 | ||||
chr1:19287902-19288144 | Rare:63 | ||||
chr1:19294012-19294282 | Rare:65 | ||||
chr1:19325955-19326288 | Common:2; Rare:81 | ||||
chr1:19384869-19385022 | Common:1; Rare:20 | ||||
chr1:20655484-20655665 | Common:1; Rare:55; Clinvar (benign):2 | ||||
chr1:20655778-20655866 | Rare:26; Clinvar (benign):1 |