Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93848080-93848256 | Common:2; Rare:46 | ||||
chr1:94078989-94079389 | Common:8; Rare:155; Clinvar (pathogenic):3 | ||||
chr1:94092180-94092670 | Common:3; Rare:84 | ||||
chr1:94247690-94247960 | Common:3; Rare:94 | ||||
chr1:94592287-94592938 | Common:11; Rare:174 | ||||
chr1:94661118-94661237 | Rare:15 | ||||
chr1:94854420-94854690 | Rare:58 | ||||
chr1:94865077-94865613 | Common:7; Rare:192 | ||||
chr1:94866503-94866711 | Rare:32 | ||||
chr1:94883940-94884570 | Common:8; Rare:111 | ||||
chr1:95407484-95408148 | Common:1; Rare:211 | ||||
chr1:95780830-95781200 | Common:2; Rare:63 | ||||
chr1:96116682-96117082 | Common:2; Rare:95 | ||||
chr1:96519821-96520885 | Common:6; Rare:233 | ||||
chr1:96557679-96558248 | Common:11; Rare:122 |