Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6235894-6236201 | Common:10; Rare:233 | ||||
chr1:6261023-6261216 | Common:3; Rare:67 | ||||
chr1:6393328-6393568 | Common:5; Rare:157 | ||||
chr1:6393724-6393918 | Rare:120 | ||||
chr1:6419903-6420082 | Rare:94 | ||||
chr1:6424534-6424934 | Common:9; Rare:195 | ||||
chr1:6490430-6490960 | Common:3; Rare:165; Clinvar (benign):1 | ||||
chr1:6490953-6491173 | Rare:39 | ||||
chr1:6491567-6491711 | Common:2; Rare:20; Clinvar (benign):1 | ||||
chr1:6497418-6497618 | Common:2; Rare:62 | ||||
chr1:6554439-6554649 | Common:8; Rare:131 | ||||
chr1:6579791-6580070 | Common:8; Rare:191 | ||||
chr1:6599429-6599669 | Common:2; Rare:72 | ||||
chr1:6602832-6603129 | Common:7; Rare:208 | ||||
chr1:6613448-6613789 | Common:4; Rare:234 |