Variant report

Variant	rs10083589
Chromosome Location	chr15:54469149-54469150
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10083599	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10083724	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12593199	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13329258	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13329461	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13380420	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16974298	0.85[EUR][1000 genomes]
rs1897049	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897050	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897051	0.98[EUR][1000 genomes]
rs2414296	0.85[EUR][1000 genomes]
rs28412332	0.85[EUR][1000 genomes]
rs28420735	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28542531	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28557452	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28569946	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28576113	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28755986	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7181949	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv428637	chr15:54279125-54500755	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1048374	chr15:54354984-54484623	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1043666	chr15:54415970-54548495	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1041282	chr15:54436686-54476135	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1037176	chr15:54448271-54471548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv457149	chr15:54461541-54488059	Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv569494	chr15:54461541-54488059	Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv974722	chr15:54462427-54478784	Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1043823	chr15:54468477-54532985	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 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
chromosomal regions: chr1:12345-34567

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