Variant report

Variant	rs637949
Chromosome Location	chr9:21369315-21369316
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10116540	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs10117202	0.86[EUR][1000 genomes]
rs10120117	0.84[EUR][1000 genomes]
rs10122881	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10124167	0.84[EUR][1000 genomes]
rs10738591	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs10757199	0.85[CEU][hapmap]
rs10811497	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs10811527	0.84[EUR][1000 genomes]
rs10811529	0.84[EUR][1000 genomes]
rs10964878	0.86[CEU][hapmap]
rs10964884	0.85[CEU][hapmap]
rs10964885	0.86[CEU][hapmap]
rs10964896	0.86[CEU][hapmap]
rs10964918	0.86[CEU][hapmap]
rs10964920	0.86[CEU][hapmap]
rs10964930	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs10964932	0.86[CEU][hapmap]
rs10964934	0.86[CEU][hapmap]
rs10964943	0.81[EUR][1000 genomes]
rs10964952	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10964957	0.93[CEU][hapmap];0.80[TSI][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10964959	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10964961	0.84[EUR][1000 genomes]
rs1112783	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12551190	0.86[CEU][hapmap]
rs12553763	0.86[CEU][hapmap]
rs12553910	0.81[EUR][1000 genomes]
rs12555631	0.85[CEU][hapmap]
rs1330312	0.84[EUR][1000 genomes]
rs1330314	0.93[CEU][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes]
rs1411436	0.86[CEU][hapmap]
rs1424854	0.92[CEU][hapmap]
rs1590897	0.84[EUR][1000 genomes]
rs16938392	0.84[CEU][hapmap]
rs1820313	0.86[CEU][hapmap]
rs1831391	0.85[CEU][hapmap]
rs1834247	0.86[CEU][hapmap]
rs1854700	0.86[CEU][hapmap]
rs1928854	0.86[CEU][hapmap]
rs1952690	0.82[EUR][1000 genomes]
rs2015345	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs2098814	0.86[CEU][hapmap]
rs2988573	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2988574	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2990140	0.90[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2990141	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs3750479	0.86[CEU][hapmap]
rs3758236	0.93[CEU][hapmap]
rs3955236	0.86[CEU][hapmap]
rs4568686	0.84[EUR][1000 genomes]
rs4582643	0.93[CEU][hapmap];0.81[GIH][hapmap];0.85[MEX][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs4628333	0.86[CEU][hapmap]
rs4977682	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs4977684	0.86[CEU][hapmap]
rs4977714	0.82[EUR][1000 genomes]
rs4978114	0.85[CEU][hapmap]
rs57371737	0.87[EUR][1000 genomes]
rs583396	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs596180	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs597440	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs604762	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[CHD][hapmap];0.81[GIH][hapmap];0.90[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs612966	0.93[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs614541	0.93[CEU][hapmap];0.83[CHB][hapmap];0.85[CHD][hapmap];0.81[GIH][hapmap];0.90[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs617881	0.86[EUR][1000 genomes]
rs618507	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs637700	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs647167	0.86[EUR][1000 genomes]
rs653778	1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs660675	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs662831	0.86[EUR][1000 genomes]
rs667214	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs667635	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs674189	0.86[EUR][1000 genomes]
rs681680	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7019617	0.83[CEU][hapmap]
rs7019739	0.85[CEU][hapmap]
rs7030705	0.86[CEU][hapmap]
rs7031048	0.93[CEU][hapmap];0.82[TSI][hapmap]
rs7033839	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs7035639	0.86[CEU][hapmap]
rs7037147	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs7041635	0.85[CEU][hapmap]
rs7047811	0.85[CEU][hapmap]
rs768849	0.86[CEU][hapmap]
rs7849623	0.86[CEU][hapmap]
rs7849862	0.86[CEU][hapmap];0.81[GIH][hapmap]
rs7854247	0.85[CEU][hapmap]
rs7866359	0.86[CEU][hapmap]
rs7866640	0.86[EUR][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	nsv892724	chr9:20690244-21517302	Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases
2	nsv892736	chr9:21327141-21391698	Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv892737	chr9:21352862-21408824	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2752289	chr9:21361957-21499624	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv972300	chr9:21367212-21369885	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs637949	KLHL9	cis	multi-tissue	Pritchard

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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