Variant report

Variant	rs1800291
Chromosome Location	chrX:154158285-154158286
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12398789	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1467061	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1509787	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17328181	1.00[JPT][hapmap]
rs1936642	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5945116	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5945122	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5945249	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5945258	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7053448	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7058826	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7061362	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7063915	1.00[CHB][hapmap];1.00[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154153200-154209000	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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