Variant report

Variant	rs10249877
Chromosome Location	chr7:104295324-104295325
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10241057	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs10487221	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10487222	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10953439	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12537797	0.96[CEU][hapmap];0.81[CHB][hapmap];0.92[JPT][hapmap]
rs4513902	0.96[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6943307	0.96[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap]
rs7781331	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7782065	0.96[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap]
rs7801387	0.87[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]

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	nsv1024532	chr7:104281393-104299847	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104290400-104295600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:104291000-104295600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:104292000-104296000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:104295000-104295600	Enhancers	Brain Germinal Matrix	brain

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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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