Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18659692-18660289 | Common:9; Rare:259 | ||||
chr10:19816000-19816480 | Common:7; Rare:107 | ||||
chr10:21173351-21173751 | Common:3; Rare:102; Clinvar (benign):1 | ||||
chr10:21173727-21174127 | Common:4; Rare:114; Clinvar (benign):2 | ||||
chr10:21174039-21174152 | Rare:27 | ||||
chr10:21174055-21174899 | Common:8; Rare:517 | ||||
chr10:21496360-21497260 | Common:5; Rare:538 | ||||
chr10:21497161-21497708 | Common:8; Rare:218 | ||||
chr10:21516981-21517810 | Common:12; Rare:521 | ||||
chr10:21523883-21527280 | Common:33; Rare:3080 | ||||
chr10:21533536-21533685 | Rare:43 | ||||
chr10:21533858-21534865 | Common:20; Rare:1512 | ||||
chr10:21534807-21535380 | Common:10; Rare:511 | ||||
chr10:22003130-22003997 | Common:14; Rare:839 | ||||
chr10:22315516-22315916 | Rare:86 |