Variant report

Variant	rs7763064
Chromosome Location	chr6:142797289-142797290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1040525	0.88[CEU][hapmap];0.81[CHB][hapmap];0.89[GIH][hapmap];0.89[MEX][hapmap];0.86[TSI][hapmap];0.90[EUR][1000 genomes]
rs1040526	0.84[CEU][hapmap];0.82[CHB][hapmap];0.86[YRI][hapmap];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1342060	0.84[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs1360194	0.84[CEU][hapmap];0.82[CHB][hapmap];0.97[GIH][hapmap];0.89[MEX][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1418201	0.84[CEU][hapmap];0.85[CHB][hapmap];0.86[EUR][1000 genomes]
rs155259	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1891308	0.94[CEU][hapmap];0.85[CHB][hapmap];0.97[GIH][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs2039986	0.84[CEU][hapmap];0.86[CHB][hapmap];0.86[EUR][1000 genomes]
rs2039987	0.81[CEU][hapmap];0.83[EUR][1000 genomes]
rs2050157	0.94[CEU][hapmap];0.81[CHB][hapmap];0.97[GIH][hapmap];0.84[MEX][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs2294764	0.84[CEU][hapmap];0.89[YRI][hapmap];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2294771	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs262115	0.86[EUR][1000 genomes]
rs262119	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs262121	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs262129	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263178	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs263179	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs263180	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263181	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263182	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263183	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263184	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263185	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs263186	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263187	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs263188	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs263189	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3748069	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3817929	0.82[CHB][hapmap];0.81[YRI][hapmap];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4896582	0.82[CEU][hapmap];0.84[EUR][1000 genomes]
rs611802	0.90[EUR][1000 genomes]
rs6570507	0.94[CEU][hapmap];0.86[CHB][hapmap];0.97[GIH][hapmap];0.88[TSI][hapmap];0.90[EUR][1000 genomes]
rs6570508	0.81[GIH][hapmap];0.85[EUR][1000 genomes]
rs6570509	0.89[CEU][hapmap];0.86[CHB][hapmap];0.92[EUR][1000 genomes]
rs6570510	0.94[CEU][hapmap];0.83[JPT][hapmap];0.84[YRI][hapmap];0.94[EUR][1000 genomes]
rs6909857	0.83[CEU][hapmap];0.81[CHB][hapmap];0.91[EUR][1000 genomes]
rs6929442	0.87[YRI][hapmap];0.94[EUR][1000 genomes]
rs6937121	0.84[CEU][hapmap];0.86[CHB][hapmap];0.94[GIH][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs7741741	0.86[CHB][hapmap];0.86[EUR][1000 genomes]
rs7753012	0.86[TSI][hapmap]
rs7754638	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7755109	0.82[CHB][hapmap];0.94[GIH][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap];0.94[EUR][1000 genomes]
rs7756305	0.84[CEU][hapmap];0.89[GIH][hapmap];0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs7770386	0.93[EUR][1000 genomes]
rs7774095	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs7776375	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9373346	0.94[CEU][hapmap];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9389984	0.82[EUR][1000 genomes]
rs9389985	0.85[CHB][hapmap];0.86[EUR][1000 genomes]
rs9389986	0.94[CEU][hapmap];0.81[CHB][hapmap];0.87[EUR][1000 genomes]
rs9389987	0.85[EUR][1000 genomes]
rs9399401	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs9403380	0.85[EUR][1000 genomes]
rs9403381	0.94[CEU][hapmap];0.97[GIH][hapmap];0.89[MEX][hapmap];0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs9403382	0.88[EUR][1000 genomes]
rs9403383	0.89[CEU][hapmap];0.81[CHB][hapmap];0.97[GIH][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs9403387	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9496346	0.86[CHB][hapmap];0.94[GIH][hapmap];0.83[MEX][hapmap];0.88[TSI][hapmap];0.87[EUR][1000 genomes]
rs9496369	0.91[EUR][1000 genomes]
rs9496374	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9496392	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs962554	0.82[CHB][hapmap];0.86[YRI][hapmap];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs972982	0.84[CEU][hapmap];0.81[CHB][hapmap];0.94[GIH][hapmap];0.88[TSI][hapmap];0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

Variant related diseases (count:2)

Disease	PMID	Source
Birth length	25281659	GWAS catalog
Height	20881960	GWAS catalog

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142796000-142806200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:142796400-142799000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:142796400-142799200	Weak transcription	Dnd41	blood

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