Variant report

Variant	rs4702110
Chromosome Location	chr5:15784914-15784915
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10434653	0.83[EUR][1000 genomes]
rs10434654	0.83[EUR][1000 genomes]
rs10462597	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10520823	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12515169	0.83[EUR][1000 genomes]
rs12515445	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12516275	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12517648	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12518052	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12519070	0.81[AMR][1000 genomes]
rs12520066	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12522526	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12522561	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12655750	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1505040	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16867549	0.81[AMR][1000 genomes]
rs16867589	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17647886	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17647898	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17704227	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17704245	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4296803	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4377704	0.83[EUR][1000 genomes]
rs4391162	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4593267	0.83[EUR][1000 genomes]
rs4701643	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58804518	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58818319	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59041652	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59800782	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73752499	0.81[AMR][1000 genomes]
rs73755514	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73755515	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73755516	0.83[EUR][1000 genomes]
rs73755517	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9637827	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9637832	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9790923	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516929	chr5:15087791-15870300	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1023068	chr5:15095221-15863583	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv869040	chr5:15097602-15866117	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv530222	chr5:15151662-15851485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830214	chr5:15589809-15791032	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv3507774	chr5:15593461-15822407	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv3507776	chr5:15593461-15822407	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1028089	chr5:15636285-15883910	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv537676	chr5:15636285-15883910	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1024248	chr5:15638067-15863583	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv537677	chr5:15638067-15863583	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv880755	chr5:15670377-15938553	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
13	esv2757107	chr5:15678556-15810987	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv2759327	chr5:15678556-15810987	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	esv2763894	chr5:15714022-15863332	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv1031483	chr5:15738485-15926083	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15764200-15796800	Weak transcription	Aorta	Aorta
2	chr5:15781000-15788600	Weak transcription	Fetal Stomach	stomach
3	chr5:15782600-15789400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:15783200-15786400	Enhancers	Left Ventricle	heart
5	chr5:15783600-15785000	Weak transcription	Fetal Muscle Leg	muscle
6	chr5:15783800-15785200	Weak transcription	Spleen	Spleen
7	chr5:15784000-15785400	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr5:15784200-15785400	Weak transcription	Right Atrium	heart
9	chr5:15784200-15792800	Weak transcription	Ovary	ovary
10	chr5:15784400-15786200	Enhancers	Fetal Heart	heart
11	chr5:15784600-15785400	Enhancers	Right Ventricle	heart
12	chr5:15784600-15785600	Enhancers	Brain Germinal Matrix	brain
13	chr5:15784600-15786000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:15784600-15787200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:15784600-15787200	Enhancers	Fetal Brain Male	brain
16	chr5:15784800-15785400	Enhancers	Brain Anterior Caudate	brain
17	chr5:15784800-15785600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:15784800-15787400	Enhancers	Cortex derived primary cultured neurospheres	brain

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