Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:94601667-94601945 | Common:2; Rare:87 | ||||
chr13:95301349-95301574 | Common:1; Rare:61 | ||||
chr13:95676930-95677229 | Common:3; Rare:104 | ||||
chr13:96053367-96053536 | Common:2; Rare:70 | ||||
chr13:97222196-97222402 | Rare:34 | ||||
chr13:98977915-98978094 | Common:2; Rare:44 | ||||
chr13:98978320-98978603 | Common:3; Rare:42 | ||||
chr13:99200638-99200896 | Common:7; Rare:114 | ||||
chr13:100088894-100089117 | Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674810-100675155 | Common:4; Rare:144 | ||||
chr13:102596806-102597035 | Common:1; Rare:110 | ||||
chr13:102773720-102773892 | Common:1; Rare:76 | ||||
chr13:102798945-102799124 | Common:1; Rare:39 | ||||
chr13:102845681-102845894 | Common:6; Rare:67; Clinvar (benign):3 | ||||
chr13:106568063-106568267 | Rare:61 |