Variant report

Variant	rs2237395
Chromosome Location	chr7:39465638-39465639
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10239767	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10239968	0.87[CEU][hapmap]
rs10242113	0.82[CEU][hapmap]
rs10261831	0.81[CEU][hapmap]
rs10262012	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10268273	0.87[CEU][hapmap]
rs10269203	0.94[CEU][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10269280	0.95[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1155269	0.87[CEU][hapmap]
rs11769625	0.81[AMR][1000 genomes]
rs11972350	0.84[CEU][hapmap]
rs11979059	0.84[CEU][hapmap]
rs12112809	0.87[CEU][hapmap]
rs17712872	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17769600	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17769607	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17769624	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1860115	0.95[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2024100	0.84[ASW][hapmap];0.90[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2073540	0.87[CEU][hapmap];0.84[LWK][hapmap];0.94[MEX][hapmap];0.84[TSI][hapmap]
rs2073542	0.82[CEU][hapmap]
rs2073543	0.82[CEU][hapmap];0.84[TSI][hapmap]
rs2073544	0.87[CEU][hapmap];0.94[MEX][hapmap];0.84[TSI][hapmap]
rs2073546	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2108719	0.90[CEU][hapmap]
rs2108720	0.87[CEU][hapmap];0.88[MEX][hapmap];0.81[TSI][hapmap]
rs2159154	0.86[CEU][hapmap]
rs2190888	0.87[CEU][hapmap]
rs2190890	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2190891	0.95[CEU][hapmap];0.84[GIH][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2215138	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237369	0.82[CEU][hapmap]
rs2237370	0.87[CEU][hapmap];0.88[MEX][hapmap]
rs2237371	0.87[CEU][hapmap];0.88[MEX][hapmap]
rs2237373	0.82[CEU][hapmap]
rs2237374	0.82[CEU][hapmap]
rs2237378	0.87[CEU][hapmap];0.88[MEX][hapmap];0.81[TSI][hapmap]
rs2237380	0.87[CEU][hapmap]
rs2237382	0.87[CEU][hapmap]
rs2237383	0.87[CEU][hapmap]
rs2237390	0.87[CEU][hapmap]
rs2237391	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2237393	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2237402	0.91[ASN][1000 genomes]
rs2282917	0.86[CEU][hapmap];0.86[MEX][hapmap];0.83[TSI][hapmap]
rs2282918	0.86[CEU][hapmap]
rs2299123	0.87[CEU][hapmap]
rs2299127	0.87[CEU][hapmap]
rs2299128	0.86[CEU][hapmap]
rs2299129	0.95[CEU][hapmap];0.82[GIH][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2299130	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2299131	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2299132	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2299133	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2302122	0.82[CEU][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap]
rs2302123	0.87[CEU][hapmap];0.83[LWK][hapmap];0.93[MEX][hapmap];0.84[TSI][hapmap]
rs2302125	0.82[CEU][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs2876837	0.87[CEU][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap]
rs2876838	0.82[CEU][hapmap]
rs2876839	0.83[ASN][1000 genomes]
rs3819420	0.95[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3819421	0.95[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3819422	0.95[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3819423	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3819426	0.95[CEU][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57998785	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61223906	0.92[ASN][1000 genomes]
rs6462917	0.95[CEU][hapmap];0.83[YRI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs740510	0.82[CEU][hapmap]
rs7459210	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7797301	0.87[CEU][hapmap];0.88[MEX][hapmap]
rs887014	0.87[CEU][hapmap]
rs887015	0.82[CEU][hapmap]

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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv966782	chr7:39454992-39581886	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39462600-39470800	Weak transcription	Fetal Muscle Leg	muscle

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