Variant report

Variant	rs11762921
Chromosome Location	chr7:121840911-121840912
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10953952	0.86[EUR][1000 genomes]
rs11521039	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11761142	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11763733	0.85[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	0.91[AFR][1000 genomes];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]
rs12155126	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12374930	0.85[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	0.83[AFR][1000 genomes];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]
rs2019876	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2083860	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2120364	0.90[EUR][1000 genomes]
rs2120365	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs279662	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs279681	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	0.82[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	0.85[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	0.85[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	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62474298	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62474305	0.88[ASN][1000 genomes]
rs62474306	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62474307	0.85[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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121839600-121841000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr7:121839600-121845800	Weak transcription	Fetal Heart	heart
3	chr7:121840800-121841000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:121840800-121841200	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links