Variant report

Variant	rs10465725
Chromosome Location	chr1:76320098-76320099
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:76262942..76264627-chr1:76319779..76321493,2	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs11161872	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11161915	0.81[AFR][1000 genomes]
rs11162065	1.00[CEU][hapmap]
rs1144329	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1144331	0.82[YRI][hapmap]
rs1144337	0.81[YRI][hapmap]
rs1144342	0.82[YRI][hapmap]
rs1146594	1.00[CEU][hapmap]
rs1146603	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1146605	0.92[EUR][1000 genomes]
rs1146606	0.92[EUR][1000 genomes]
rs1146608	0.92[EUR][1000 genomes]
rs1146611	0.92[EUR][1000 genomes]
rs1146612	0.92[EUR][1000 genomes]
rs1146614	0.92[EUR][1000 genomes]
rs1146615	0.92[EUR][1000 genomes]
rs1146618	0.92[EUR][1000 genomes]
rs1146619	0.92[EUR][1000 genomes]
rs1146620	0.92[EUR][1000 genomes]
rs1146622	0.92[EUR][1000 genomes]
rs1146624	0.92[EUR][1000 genomes]
rs1146628	0.92[EUR][1000 genomes]
rs1146629	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1146641	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1146651	0.82[YRI][hapmap]
rs12074938	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12079065	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12079211	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12079950	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12081631	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12086506	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12089337	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs12090389	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12093817	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12094698	0.92[EUR][1000 genomes]
rs12164500	0.83[YRI][hapmap]
rs1251274	0.82[YRI][hapmap]
rs13376397	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17097567	1.00[CEU][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17097696	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17097707	1.00[CEU][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs17097710	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3795251	0.93[YRI][hapmap]
rs55781251	0.91[EUR][1000 genomes]
rs55977041	1.00[EUR][1000 genomes]
rs56322662	1.00[EUR][1000 genomes]
rs56364153	0.91[EUR][1000 genomes]
rs57443433	1.00[EUR][1000 genomes]
rs5745309	1.00[CEU][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5745392	0.82[YRI][hapmap]
rs5745418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5745496	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5745516	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5745542	0.93[YRI][hapmap]
rs57798497	1.00[EUR][1000 genomes]
rs58125729	1.00[EUR][1000 genomes]
rs59723961	1.00[EUR][1000 genomes]
rs59932454	1.00[EUR][1000 genomes]
rs60219146	0.91[EUR][1000 genomes]
rs61124994	0.84[EUR][1000 genomes]
rs61612438	1.00[EUR][1000 genomes]
rs61676733	0.88[AFR][1000 genomes]
rs6692903	1.00[CEU][hapmap]
rs74088996	0.91[EUR][1000 genomes]
rs74088997	0.91[EUR][1000 genomes]
rs74088999	0.91[EUR][1000 genomes]
rs74090705	0.91[EUR][1000 genomes]
rs74090716	1.00[EUR][1000 genomes]
rs74090717	1.00[EUR][1000 genomes]
rs74090720	1.00[EUR][1000 genomes]
rs74090724	1.00[EUR][1000 genomes]
rs74090726	1.00[EUR][1000 genomes]
rs74090729	1.00[EUR][1000 genomes]
rs74090734	1.00[EUR][1000 genomes]
rs74090737	1.00[EUR][1000 genomes]
rs74090744	1.00[EUR][1000 genomes]
rs7512465	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7544911	0.84[EUR][1000 genomes]
rs815310	0.82[EUR][1000 genomes]
rs815311	0.82[EUR][1000 genomes]
rs9970840	1.00[CEU][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1795237	chr1:76268573-76383565	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1800125	chr1:76269439-76379497	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1799260	chr1:76269439-76383297	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1847721	chr1:76269439-76383565	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1004669	chr1:76301198-76409451	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv871671	chr1:76304215-76391646	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76319600-76327400	Weak transcription	Aorta	Aorta
2	chr1:76319800-76320200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:76320000-76320400	Enhancers	Hela-S3	cervix
4	chr1:76320000-76320400	Enhancers	HMEC	breast
5	chr1:76320000-76320800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:76320000-76321400	Enhancers	HepG2	liver
7	chr1:76320000-76321400	Enhancers	K562	blood

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