Variant report

Variant	rs2019876
Chromosome Location	chr7:121837835-121837836
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10953952	0.86[EUR][1000 genomes]
rs11521039	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11761142	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11762921	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11765219	0.81[EUR][1000 genomes]
rs11766185	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11772230	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1206207	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1206353	0.81[JPT][hapmap]
rs1206376	0.86[JPT][hapmap]
rs12155126	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12374930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs157653	0.86[EUR][1000 genomes]
rs1604332	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17144133	0.82[ASN][1000 genomes]
rs1995328	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2083860	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2120364	0.90[EUR][1000 genomes]
rs2120365	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs279662	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs279667	0.80[CHB][hapmap]
rs279681	0.82[CEU][hapmap];0.81[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs279687	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs279693	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs279698	0.89[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55818404	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56177919	0.86[ASN][1000 genomes]
rs56318514	0.84[EUR][1000 genomes]
rs56331846	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57562127	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58850466	0.86[ASN][1000 genomes]
rs59536307	0.88[EUR][1000 genomes]
rs60116323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61366730	0.88[EUR][1000 genomes]
rs62474297	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62474298	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62474305	0.88[ASN][1000 genomes]
rs62474306	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62474307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6959778	0.89[EUR][1000 genomes]
rs73226275	0.86[ASN][1000 genomes]
rs7802078	0.84[AMR][1000 genomes];0.90[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	nsv427803	chr7:121701581-121876302	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1034624	chr7:121813180-121899703	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1034797	chr7:121815255-121897109	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1028221	chr7:121818974-121899162	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1024868	chr7:121818974-121899703	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121832000-121838600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:121834000-121838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:121834800-121839400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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