Variant report

Variant	rs967920
Chromosome Location	chr7:104048754-104048755
allele	A/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:12)

rs_ID	r²[population]
rs1014557	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs10487205	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10487206	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10487208	1.00[YRI][hapmap]
rs16869746	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs17137313	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17137377	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17137382	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2188484	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4605995	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6952192	0.86[ASN][1000 genomes]
rs967919	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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

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