Variant report

Variant	rs11162483
Chromosome Location	chr1:78855422-78855423
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10489786	0.93[YRI][hapmap];0.87[AFR][1000 genomes]
rs1156032	1.00[ASW][hapmap];0.81[LWK][hapmap];0.92[AFR][1000 genomes]
rs1265657	1.00[AMR][1000 genomes]
rs1265663	1.00[AMR][1000 genomes]
rs1322930	1.00[AMR][1000 genomes]
rs1322932	1.00[AMR][1000 genomes]
rs1322936	1.00[AMR][1000 genomes]
rs1332255	0.87[AFR][1000 genomes]
rs1332256	0.91[YRI][hapmap];0.87[AFR][1000 genomes]
rs1333979	1.00[AMR][1000 genomes]
rs1412846	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17101751	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17101783	1.00[AMR][1000 genomes]
rs1888894	0.93[YRI][hapmap];0.87[AFR][1000 genomes]
rs1888895	0.93[YRI][hapmap];0.87[AFR][1000 genomes]
rs1888896	0.86[YRI][hapmap];0.83[AFR][1000 genomes]
rs2149032	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs2352036	1.00[ASW][hapmap];0.86[MKK][hapmap]
rs4650347	0.98[AFR][1000 genomes]
rs487376	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs489704	0.81[YRI][hapmap]
rs494131	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs540676	0.81[YRI][hapmap]
rs553310	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs559854	1.00[AMR][1000 genomes]
rs564407	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs569846	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs574426	0.84[AFR][1000 genomes]
rs576056	0.87[YRI][hapmap];0.84[AFR][1000 genomes]
rs581338	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs599583	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs601137	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs602865	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs626770	0.98[AFR][1000 genomes]
rs640003	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6424768	0.92[AFR][1000 genomes]
rs6424769	0.96[AFR][1000 genomes]
rs645528	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs663485	1.00[AMR][1000 genomes]
rs664465	0.87[YRI][hapmap];0.84[AFR][1000 genomes]
rs676130	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs689110	1.00[AMR][1000 genomes]
rs7516567	0.85[LWK][hapmap];1.00[AMR][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	nsv1013008	chr1:78463173-78958701	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv535012	chr1:78463173-78958701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv482697	chr1:78786028-78935333	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	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
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