Variant report

Variant	rs10920664
Chromosome Location	chr1:190202167-190202168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10800940	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10920656	1.00[AMR][1000 genomes]
rs10920657	1.00[AMR][1000 genomes]
rs10920667	0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10920685	0.85[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10920695	1.00[AMR][1000 genomes]
rs12060718	0.83[YRI][hapmap]
rs12061471	1.00[AMR][1000 genomes]
rs12062310	1.00[AMR][1000 genomes]
rs12063934	0.92[YRI][hapmap]
rs12067650	1.00[AMR][1000 genomes]
rs12069314	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12070897	1.00[AMR][1000 genomes]
rs12074400	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12078989	1.00[AMR][1000 genomes]
rs12079649	1.00[AMR][1000 genomes]
rs12080072	1.00[AMR][1000 genomes]
rs12080920	1.00[AMR][1000 genomes]
rs12082166	1.00[AMR][1000 genomes]
rs12084800	1.00[AMR][1000 genomes]
rs12086633	1.00[AMR][1000 genomes]
rs12087388	1.00[AMR][1000 genomes]
rs12088760	1.00[AMR][1000 genomes]
rs12090663	1.00[AMR][1000 genomes]
rs12090807	1.00[AMR][1000 genomes]
rs12093281	1.00[AMR][1000 genomes]
rs12096195	1.00[AMR][1000 genomes]
rs12097847	1.00[AMR][1000 genomes]
rs16832207	0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][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	nsv548532	chr1:189758772-190371671	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917005	chr1:189855484-190259380	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv932040	chr1:190005334-190914580	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1003035	chr1:190123195-190291554	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv872756	chr1:190164775-190287713	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1013402	chr1:190197674-190332464	Enhancers ZNF genes & repeats Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
7	nsv535246	chr1:190197674-190332464	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190196800-190204200	Weak transcription	Fetal Intestine Small	intestine

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