Variant report

Variant	rs9451569
Chromosome Location	chr6:91781599-91781600
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11962583	0.91[ASN][1000 genomes]
rs11966543	0.91[ASN][1000 genomes]
rs16883967	1.00[ASN][1000 genomes]
rs16883969	1.00[ASN][1000 genomes]
rs16883970	1.00[ASN][1000 genomes]
rs16883972	0.91[ASN][1000 genomes]
rs4492171	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62417844	0.91[ASN][1000 genomes]
rs6901237	0.91[ASN][1000 genomes]
rs6907560	1.00[ASN][1000 genomes]
rs6912628	0.91[ASN][1000 genomes]
rs6913089	0.91[ASN][1000 genomes]
rs6913485	0.91[ASN][1000 genomes]
rs6913588	1.00[ASN][1000 genomes]
rs6924218	0.91[ASN][1000 genomes]
rs6924814	0.91[ASN][1000 genomes]
rs6925219	0.91[ASN][1000 genomes]
rs6938432	0.91[ASN][1000 genomes]
rs7766974	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523939	chr6:91067623-91790493	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2752130	chr6:91740447-92196479	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv830726	chr6:91750692-91921838	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:91779800-91784000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:91781200-91789600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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