Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45750607-45750856 | Rare:89 | ||||
chr1:46198347-46198534 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303126-46303769 | Common:3; Rare:192 | ||||
chr1:46340647-46340828 | Common:3; Rare:52 | ||||
chr1:46616825-46617027 | Common:2; Rare:44 | ||||
chr1:47314093-47314511 | Common:3; Rare:94; Clinvar:1 | ||||
chr1:47333773-47333984 | Common:2; Rare:72 | ||||
chr1:50970097-50970271 | Rare:33 | ||||
chr1:51236749-51236876 | Rare:35 | ||||
chr1:51878586-51879000 | Common:1; Rare:120 | ||||
chr1:52055130-52055320 | Common:1; Rare:48 | ||||
chr1:52055659-52055810 | Common:1; Rare:22 | ||||
chr1:52056136-52056359 | Rare:66 | ||||
chr1:52404448-52404624 | Common:1; Rare:53 | ||||
chr1:52553071-52553377 | Common:4; Rare:84 |