Variant report

Variant	rs57105102
Chromosome Location	chr3:28790824-28790825
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10460988	0.88[EUR][1000 genomes]
rs11129327	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11129329	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11922784	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13319272	0.80[AFR][1000 genomes]
rs13326317	0.80[AFR][1000 genomes]
rs17021863	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17021907	0.81[EUR][1000 genomes]
rs28637755	0.80[AFR][1000 genomes]
rs55803909	0.87[EUR][1000 genomes]
rs57255761	0.80[AFR][1000 genomes]
rs6775238	0.85[AFR][1000 genomes]
rs6795363	0.86[EUR][1000 genomes]
rs6807704	0.81[EUR][1000 genomes]
rs73068811	0.89[EUR][1000 genomes]
rs73068812	0.89[EUR][1000 genomes]
rs73068820	0.89[EUR][1000 genomes]
rs73068823	0.89[EUR][1000 genomes]
rs73068851	0.89[EUR][1000 genomes]
rs7428667	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv916364	chr3:28468275-29146280	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv876651	chr3:28774258-28823156	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
4	nsv590011	chr3:28780713-29044437	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28788800-28796400	Weak transcription	Left Ventricle	heart
2	chr3:28790400-28792000	Weak transcription	Psoas Muscle	Psoas

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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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