Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:105854403-105854740 | Rare:113 | ||||
chr14:105854908-105855237 | Common:3; Rare:96 | ||||
chr14:105855478-105855829 | Common:3; Rare:124 | ||||
chr14:105855866-105856301 | Common:6; Rare:147; Clinvar (benign):2 | ||||
chr14:105856666-105856827 | Common:1; Rare:23 | ||||
chr14:105856992-105857327 | Common:1; Rare:74 | ||||
chr14:105858165-105858433 | Common:4; Rare:80 | ||||
chr14:105858824-105858937 | Rare:47 | ||||
chr14:105859134-105859235 | Rare:47 | ||||
chr14:105859244-105859341 | Rare:37 | ||||
chr14:105859555-105859753 | Common:2; Rare:88 | ||||
chr14:105859811-105859844 | Rare:19 | ||||
chr14:105860120-105860207 | Rare:28 | ||||
chr14:105860349-105860455 | Rare:59 | ||||
chr14:105860503-105860667 | Common:2; Rare:94 |