Variant report

Variant	rs9981948
Chromosome Location	chr21:37945560-37945561
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:11)

rs_ID	r²[population]
rs10854378	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11088357	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11702057	0.87[ASN][1000 genomes]
rs12626551	0.87[ASN][1000 genomes]
rs2835402	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61153775	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61197907	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7276044	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs743426	0.87[ASN][1000 genomes]
rs9941880	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9977315	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834090	chr21:37812545-38009542	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1064290	chr21:37878964-37983133	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:37944800-37952400	Weak transcription	Fetal Muscle Leg	muscle

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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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