Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35122885-35122991 | Rare:24 | ||||
chr14:35292198-35292479 | Common:5; Rare:105; Clinvar:1 | ||||
chr14:35402705-35403238 | Common:6; Rare:173; Clinvar (benign):4 | ||||
chr14:35403721-35404059 | Rare:115; Clinvar:1; Clinvar (benign):2 | ||||
chr14:35404423-35404954 | Common:3; Rare:160; Clinvar:1; Clinvar (benign):5 | ||||
chr14:37172092-37172138 | Rare:13 | ||||
chr14:37172343-37172413 | Rare:34 | ||||
chr14:37197858-37198092 | Common:3; Rare:76 | ||||
chr14:38256056-38256179 | Common:1; Rare:32 | ||||
chr14:39114137-39114334 | Common:2; Rare:61 | ||||
chr14:39174970-39175289 | Common:4; Rare:111 | ||||
chr14:39266868-39267428 | Common:3; Rare:195 | ||||
chr14:39432447-39432657 | Common:6; Rare:74 | ||||
chr14:44897065-44897346 | Common:1; Rare:100 | ||||
chr14:44961892-44962278 | Common:3; Rare:111 |