Variant report

Variant	rs28715379
Chromosome Location	chrX:154123809-154123810
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000207165	Chromatin interaction
ENSG00000224069	Chromatin interaction
ENSG00000013563	Chromatin interaction
ENSG00000147403	Chromatin interaction

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154116200-154131000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chrX:154120800-154134800	Weak transcription	Left Ventricle	heart

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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