Variant report

Variant	rs2658778
Chromosome Location	chr11:93148948-93148949
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10466368	0.86[EUR][1000 genomes]
rs11601056	0.87[EUR][1000 genomes]
rs11604909	0.85[CEU][hapmap];0.95[GIH][hapmap];0.82[TSI][hapmap];0.87[EUR][1000 genomes]
rs1456238	0.86[CEU][hapmap];0.92[JPT][hapmap];0.83[EUR][1000 genomes]
rs1563445	0.82[ASW][hapmap];0.83[TSI][hapmap]
rs1869914	0.86[CEU][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.80[LWK][hapmap];0.84[MEX][hapmap];0.83[EUR][1000 genomes]
rs1975820	0.92[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs2019814	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2259633	0.86[CEU][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.84[MEX][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2446061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2605574	0.80[CEU][hapmap];0.94[CHD][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2605580	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2605581	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2605583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2605611	0.91[ASW][hapmap];0.85[CEU][hapmap];0.95[GIH][hapmap];0.86[EUR][1000 genomes]
rs2605626	0.82[ASW][hapmap]
rs2608214	0.91[ASW][hapmap];0.93[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.92[MEX][hapmap];0.91[TSI][hapmap]
rs2608215	0.93[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2658773	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2658775	0.86[CEU][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.83[LWK][hapmap];0.84[MEX][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2658776	0.86[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs2658777	0.92[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs2658779	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap]
rs2658781	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap]
rs2658782	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2658791	0.92[EUR][1000 genomes]
rs2925355	1.00[ASW][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.81[LWK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs2925362	0.82[EUR][1000 genomes]
rs2925938	0.83[EUR][1000 genomes]
rs3019205	0.83[EUR][1000 genomes]
rs3019206	0.83[EUR][1000 genomes]
rs3019221	0.88[CHD][hapmap];0.92[JPT][hapmap]
rs3019222	0.81[EUR][1000 genomes]
rs3019223	0.81[EUR][1000 genomes]
rs3020057	0.86[CEU][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.84[MEX][hapmap];0.83[EUR][1000 genomes]
rs3020073	0.89[CHD][hapmap];0.83[EUR][1000 genomes]
rs3020076	0.85[EUR][1000 genomes]
rs56091149	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7116173	0.86[EUR][1000 genomes]
rs72972357	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72972364	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv1035530	chr11:93114111-93148948	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv555941	chr11:93129893-93181050	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv439	chr11:93135936-93171682	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv508649	chr11:93140899-93181092	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1039623	chr11:93141461-93328739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2658778	CCDC67	cis	Thyroid	GTEx

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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