Variant report

Variant	rs12434471
Chromosome Location	chr14:22160553-22160554
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10148566	0.84[ASN][1000 genomes]
rs12431503	1.00[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap]
rs12589185	0.80[ASN][1000 genomes]
rs12589513	1.00[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs12589962	0.80[ASN][1000 genomes]
rs12894518	0.84[ASN][1000 genomes]
rs17182761	0.80[ASN][1000 genomes]
rs2204931	0.83[EUR][1000 genomes]
rs2319874	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2319875	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35762321	0.85[EUR][1000 genomes]
rs4628878	0.80[ASN][1000 genomes]
rs4982482	0.81[EUR][1000 genomes]
rs4982483	0.80[EUR][1000 genomes]
rs4982486	1.00[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.91[YRI][hapmap]
rs4982487	1.00[CEU][hapmap];0.93[JPT][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55654479	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59305233	0.89[AFR][1000 genomes]
rs6650488	1.00[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs7143458	0.87[JPT][hapmap]
rs7143695	0.85[ASN][1000 genomes]
rs7148008	0.93[JPT][hapmap]
rs7158141	0.80[ASN][1000 genomes]
rs725891	0.87[YRI][hapmap]
rs72688056	0.89[AFR][1000 genomes]
rs8006599	0.81[JPT][hapmap]
rs8017708	0.87[YRI][hapmap]
rs8020038	1.00[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs8020165	0.88[CHB][hapmap];0.93[JPT][hapmap]
rs8022425	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422459	chr14:21931624-22169502	Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv1042309	chr14:22042511-22866936	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
3	nsv456147	chr14:22073473-22305071	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv563851	chr14:22073473-22305071	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv510629	chr14:22134425-22215842	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 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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