Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81221295-81221471 | Common:1; Rare:43 | ||||
chr14:85530033-85530199 | Common:1; Rare:37 | ||||
chr14:90331918-90332203 | Common:1; Rare:77 | ||||
chr14:91510268-91510624 | Common:1; Rare:111 | ||||
chr14:92040019-92040152 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr14:92121673-92121985 | Common:4; Rare:100 | ||||
chr14:93184876-93184996 | Rare:37 | ||||
chr14:93207024-93207284 | Common:2; Rare:128 | ||||
chr14:94081125-94081333 | Common:5; Rare:68 | ||||
chr14:95157424-95157685 | Common:4; Rare:93 | ||||
chr14:96363356-96363507 | Rare:41 | ||||
chr14:96502301-96502447 | Rare:56 | ||||
chr14:100376273-100376485 | Common:3; Rare:71 | ||||
chr14:101809748-101809886 | Rare:25 | ||||
chr14:102139747-102139914 | Rare:55 |