Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10433502	0.86[TSI][hapmap]
rs11914870	0.86[TSI][hapmap]
rs13076798	0.88[MKK][hapmap]
rs17047647	0.88[MKK][hapmap]
rs17047650	0.88[MKK][hapmap]
rs17047690	0.83[AFR][1000 genomes]
rs2136716	0.83[CHD][hapmap];0.91[MKK][hapmap]
rs2136717	0.90[AFR][1000 genomes]
rs4277695	0.88[MKK][hapmap]
rs4634123	1.00[LWK][hapmap];0.95[MKK][hapmap]
rs4855480	0.90[AFR][1000 genomes]
rs4855482	1.00[ASW][hapmap]
rs4855489	0.87[MKK][hapmap]
rs6549127	0.86[TSI][hapmap]
rs73092815	1.00[AFR][1000 genomes]
rs73092834	0.90[AFR][1000 genomes]
rs73111013	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73111015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73111018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73111023	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73111024	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7646334	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7653487	0.90[AFR][1000 genomes]
rs956352	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1003779	chr3:68470899-68517125	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7634101	FAM19A1	cis	Stomach	GTEx
rs7634101	UBA3	cis	parietal	SCAN
rs7634101	FOXP1	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68477800-68487400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:68483600-68486200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr3:68483800-68486200	Weak transcription	Colon Smooth Muscle	Colon
4	chr3:68484400-68485800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:68484600-68486200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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