Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:44361483-44361964 | Common:3; Rare:152 | ||||
chr2:46617019-46617261 | Common:6; Rare:105 | ||||
chr2:46915734-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
chr2:47345045-47345148 | Rare:26 | ||||
chr2:47369256-47369556 | Common:4; Rare:129; Clinvar:10; Clinvar (benign):5 | ||||
chr2:47402911-47403194 | Common:1; Rare:127; Clinvar:42; Clinvar (benign):26 | ||||
chr2:47905496-47905877 | Common:3; Rare:186 | ||||
chr2:48314345-48314764 | Rare:153 | ||||
chr2:48440631-48440858 | Common:7; Rare:111 | ||||
chr2:51032014-51032297 | Common:1; Rare:67; Clinvar:3 | ||||
chr2:51032427-51032546 | Common:7; Rare:27; Clinvar:4 | ||||
chr2:53786842-53787078 | Rare:81 | ||||
chr2:53970788-53971188 | Common:12; Rare:144 | ||||
chr2:54456019-54456417 | Common:4; Rare:153 | ||||
chr2:55050313-55050376 | Rare:24 |