Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11623433	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs11625977	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs11627233	0.93[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11627445	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs11629254	0.93[CEU][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17107740	1.00[YRI][hapmap]
rs17107778	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs17175297	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17175346	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs17175444	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs17765078	0.82[EUR][1000 genomes]
rs41285486	0.82[EUR][1000 genomes]
rs61977411	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61977412	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61977413	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61977415	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61977417	0.83[EUR][1000 genomes]
rs61977420	0.82[EUR][1000 genomes]
rs61977422	0.82[EUR][1000 genomes]
rs61977423	0.83[EUR][1000 genomes]
rs61977424	0.83[EUR][1000 genomes]
rs61977425	0.83[EUR][1000 genomes]
rs61977426	0.83[EUR][1000 genomes]
rs7150941	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs7161025	0.82[EUR][1000 genomes]
rs8013407	0.83[EUR][1000 genomes]
rs8013867	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs8020358	0.86[CEU][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70512800-70535600	Weak transcription	Psoas Muscle	Psoas
2	chr14:70514600-70531200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr14:70526200-70527000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr14:70526400-70549000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:70526800-70529400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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