Variant report

Variant	rs2014244
Chromosome Location	chr4:101742394-101742395
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs13102244	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13104901	0.91[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13107645	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13109077	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13109446	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13109508	0.91[AFR][1000 genomes]
rs13110542	0.80[EUR][1000 genomes]
rs13110644	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13111905	0.80[EUR][1000 genomes]
rs13116153	0.80[EUR][1000 genomes]
rs13117474	1.00[CEU][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13121245	0.80[EUR][1000 genomes]
rs13121438	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13122599	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13123162	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13129721	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13130074	0.81[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13137007	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13149562	0.86[AMR][1000 genomes]
rs13150288	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs1390931	0.80[EUR][1000 genomes]
rs1390932	0.80[EUR][1000 genomes]
rs17227226	0.80[EUR][1000 genomes]
rs17813352	0.80[EUR][1000 genomes]
rs17813556	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs17813598	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs17813670	0.80[EUR][1000 genomes]
rs17813694	0.80[EUR][1000 genomes]
rs1976560	0.86[AMR][1000 genomes]
rs2202773	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2903222	0.80[EUR][1000 genomes]
rs34040983	0.81[AMR][1000 genomes]
rs34080291	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34126461	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34716852	0.80[EUR][1000 genomes]
rs34742412	0.89[CEU][hapmap];0.83[GIH][hapmap];0.81[TSI][hapmap]
rs34754564	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34802397	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34810105	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34833700	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34839174	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34891917	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34906832	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34920876	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs35024886	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs35150863	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs35170503	0.80[EUR][1000 genomes]
rs35209788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35481231	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs35485367	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35554164	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs35564595	0.80[EUR][1000 genomes]
rs35629108	0.80[EUR][1000 genomes]
rs35664627	0.80[EUR][1000 genomes]
rs35795105	1.00[AFR][1000 genomes]
rs35863364	0.80[EUR][1000 genomes]
rs36091097	0.80[EUR][1000 genomes]
rs62305804	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62305805	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62305826	0.80[EUR][1000 genomes]
rs62305828	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs62305832	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs62305833	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs62305834	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs62305843	0.80[EUR][1000 genomes]
rs62307671	0.80[EUR][1000 genomes]
rs62307674	0.80[EUR][1000 genomes]
rs62307677	0.80[EUR][1000 genomes]
rs62307678	0.80[EUR][1000 genomes]
rs62307679	0.80[EUR][1000 genomes]
rs62307680	0.80[EUR][1000 genomes]
rs7434953	0.80[EUR][1000 genomes]
rs7437932	0.80[EUR][1000 genomes]
rs7441213	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7441263	1.00[AFR][1000 genomes]
rs7441325	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7655125	0.89[CEU][hapmap]
rs931622	0.80[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931418	chr4:101500167-102443207	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:101740000-101745600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:101741200-101742600	Enhancers	GM12878-XiMat	blood
3	chr4:101741200-101744600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:101741800-101742400	Enhancers	Dnd41	blood

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