Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:44141977-44142337 | Common:6; Rare:58 | ||||
chr13:44237411-44237610 | Common:1; Rare:29 | ||||
chr13:44306911-44306926 | |||||
chr13:48413078-48413245 | Rare:19 | ||||
chr13:52194378-52194520 | Rare:43 | ||||
chr13:57629910-57630132 | Common:1; Rare:65 | ||||
chr13:76882615-76882733 | Common:1; Rare:15 | ||||
chr13:87671327-87671392 | Rare:22 | ||||
chr13:94549349-94549458 | Common:1; Rare:35 | ||||
chr13:95239948-95240079 | Common:2; Rare:29 | ||||
chr13:100438488-100438677 | Rare:30 | ||||
chr13:102394493-102394646 | Common:1; Rare:58 | ||||
chr13:110308524-110308711 | Common:1; Rare:36 | ||||
chr13:110503790-110503911 | Common:3; Rare:34; Clinvar (benign):2 | ||||
chr13:113351548-113351661 | Rare:20 |