Variant report

Variant	rs17141244
Chromosome Location	chr7:117951560-117951561
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10239120	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10953865	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10953866	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11981239	0.93[EUR][1000 genomes]
rs11982333	0.87[EUR][1000 genomes]
rs12669395	0.90[EUR][1000 genomes]
rs12674239	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17141130	0.93[EUR][1000 genomes]
rs17141139	0.93[EUR][1000 genomes]
rs17141216	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17141219	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17141231	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2402358	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34126707	0.90[EUR][1000 genomes]
rs3757800	0.87[EUR][1000 genomes]
rs4454229	0.80[EUR][1000 genomes]
rs4730861	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs57970913	0.93[EUR][1000 genomes]
rs58836778	1.00[EUR][1000 genomes]
rs59338276	0.87[EUR][1000 genomes]
rs59768076	0.83[EUR][1000 genomes]
rs60680906	1.00[EUR][1000 genomes]
rs61345178	0.88[ASN][1000 genomes]
rs61632875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6948367	0.90[EUR][1000 genomes]
rs6959973	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6973741	0.90[EUR][1000 genomes]
rs73475579	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73483487	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73716919	0.87[EUR][1000 genomes]
rs73716927	0.90[EUR][1000 genomes]
rs73716929	0.90[EUR][1000 genomes]
rs73716958	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7778764	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs973023	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv889090	chr7:117865940-118067460	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv889091	chr7:117899190-117963926	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1029103	chr7:117917362-118035987	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2764014	chr7:117917374-118035999	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv608261	chr7:117917719-117965390	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv608262	chr7:117926753-118036133	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv429805	chr7:117940049-118026049	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117949800-117955000	Enhancers	Dnd41	blood
2	chr7:117950000-117953000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr7:117951000-117952400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:117951000-117953000	Enhancers	HMEC	breast
5	chr7:117951200-117951600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr7:117951200-117952200	Weak transcription	Hela-S3	cervix
7	chr7:117951200-117952400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:117951400-117951800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:117951400-117952200	Enhancers	NHEK	skin
10	chr7:117951400-117952400	Flanking Active TSS	GM12878-XiMat	blood

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