Variant report

Variant	rs10911787
Chromosome Location	chr1:185923773-185923774
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10047250	1.00[CEU][hapmap]
rs10157843	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10489717	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10489718	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10911783	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10911784	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs10911785	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10911788	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10911789	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10911790	1.00[EUR][1000 genomes]
rs11586768	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11586771	1.00[AMR][1000 genomes]
rs11587002	1.00[EUR][1000 genomes]
rs11589455	1.00[CEU][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes]
rs11800990	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11804668	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12057384	1.00[EUR][1000 genomes]
rs12059676	0.93[AFR][1000 genomes]
rs12062879	1.00[CEU][hapmap]
rs12067376	1.00[CEU][hapmap]
rs12068599	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12068829	1.00[CEU][hapmap];0.83[YRI][hapmap];0.93[AMR][1000 genomes]
rs12073492	0.93[AMR][1000 genomes]
rs12077084	0.92[AFR][1000 genomes]
rs12088513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12088571	1.00[EUR][1000 genomes]
rs12094899	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12095309	0.94[EUR][1000 genomes]
rs1322361	1.00[CEU][hapmap];0.84[YRI][hapmap];0.93[AMR][1000 genomes]
rs1407427	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs1555494	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16824945	1.00[CEU][hapmap]
rs28535260	0.92[AFR][1000 genomes]
rs28696376	1.00[EUR][1000 genomes]
rs34427602	0.93[AFR][1000 genomes]
rs41397650	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs4288554	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs58291464	1.00[EUR][1000 genomes]
rs58610258	0.94[EUR][1000 genomes]
rs6425011	1.00[CEU][hapmap]
rs6675465	1.00[CEU][hapmap]
rs6695626	1.00[CEU][hapmap]
rs72703022	1.00[EUR][1000 genomes]
rs72703023	1.00[EUR][1000 genomes]
rs72718864	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72718865	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs72718866	1.00[EUR][1000 genomes]
rs72718867	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs72718868	1.00[EUR][1000 genomes]
rs72718870	1.00[EUR][1000 genomes]
rs7527214	1.00[CEU][hapmap]
rs7539719	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs7546152	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7552194	1.00[CEU][hapmap]

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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185895200-185932200	Weak transcription	Aorta	Aorta
2	chr1:185908600-185925200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:185922800-185924200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:185922800-185931200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:185923400-185923800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr1:185923400-185923800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr1:185923400-185923800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr1:185923400-185924400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:185923600-185923800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr1:185923600-185923800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr1:185923600-185924200	Enhancers	HUES48 Cell Line	embryonic stem cell

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