Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1103983-1104398 | Common:5; Rare:130 | ||||
chr19:1105185-1105507 | Common:1; Rare:143; Clinvar (pathogenic):1 | ||||
chr19:1173825-1173915 | Common:2; Rare:25 | ||||
chr19:1174187-1174321 | Rare:70 | ||||
chr19:1205512-1205787 | Common:1; Rare:75 | ||||
chr19:1237998-1238149 | Rare:48 | ||||
chr19:1241610-1241860 | Rare:79 | ||||
chr19:1249700-1249936 | Rare:96 | ||||
chr19:1269249-1269398 | Rare:66 | ||||
chr19:1275351-1275558 | Common:1; Rare:102 | ||||
chr19:1275767-1276131 | Common:2; Rare:164 | ||||
chr19:1354786-1355085 | Common:3; Rare:139 | ||||
chr19:1383475-1383542 | Common:1; Rare:28 | ||||
chr19:1407272-1407801 | Common:2; Rare:200 | ||||
chr19:1414978-1415240 | Rare:58 |