Variant report

Variant	rs9821724
Chromosome Location	chr3:21624920-21624921
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:21550526..21552335-chr3:21623798..21625685,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11708720	0.80[CEU][hapmap]
rs11713447	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11714683	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11928376	0.87[CEU][hapmap]
rs13068076	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13068431	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13068965	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13092094	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13099530	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28369086	0.87[EUR][1000 genomes]
rs28625100	0.83[EUR][1000 genomes]
rs34323566	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35104803	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62236078	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62236079	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62236133	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6550611	0.82[EUR][1000 genomes]
rs6550612	0.94[EUR][1000 genomes]
rs73033316	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9822059	0.87[CEU][hapmap];0.96[EUR][1000 genomes]
rs9827481	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9833976	0.93[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9841949	0.93[CEU][hapmap];0.96[EUR][1000 genomes]
rs9859649	0.93[CEU][hapmap];0.96[EUR][1000 genomes]
rs9877267	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010460	chr3:21516810-21839871	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv834631	chr3:21612283-21763887	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv589895	chr3:21622387-21638815	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1003451	chr3:21623631-21662267	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21603200-21634400	Weak transcription	Left Ventricle	heart
2	chr3:21618400-21643200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:21622800-21634400	Weak transcription	Aorta	Aorta
4	chr3:21623200-21625800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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