Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88583415-88583652 | Common:1; Rare:38 | ||||
chr10:88990424-88990877 | Common:6; Rare:119; Clinvar:1; Clinvar (benign):5 | ||||
chr10:88991056-88991104 | Rare:14 | ||||
chr10:88991126-88991362 | Common:4; Rare:51 | ||||
chr10:89327959-89328015 | Common:1; Rare:7 | ||||
chr10:89392588-89392658 | Rare:15 | ||||
chr10:89414622-89414785 | Common:3; Rare:73 | ||||
chr10:89643883-89644181 | Rare:65 | ||||
chr10:89644936-89645342 | Common:5; Rare:180 | ||||
chr10:89701376-89701670 | Common:2; Rare:94 | ||||
chr10:90858088-90858256 | Common:1; Rare:66 | ||||
chr10:91409214-91409381 | Rare:38 | ||||
chr10:91410073-91410445 | Common:5; Rare:130 | ||||
chr10:91798254-91798512 | Common:1; Rare:103 | ||||
chr10:91909099-91909178 | Rare:13 |