Variant report

Variant	rs2723510
Chromosome Location	chr7:17816639-17816640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:17816362..17819179-chr7:17820951..17822605,2	K562	blood:

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10249221	0.91[ASN][1000 genomes]
rs10264355	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10264445	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10264447	0.91[ASN][1000 genomes]
rs1357796	0.89[YRI][hapmap]
rs1404414	0.86[LWK][hapmap];0.85[YRI][hapmap]
rs1404416	1.00[ASN][1000 genomes]
rs1404417	1.00[ASN][1000 genomes]
rs1404418	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1404419	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1404421	0.97[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1404422	0.92[MKK][hapmap]
rs1404425	0.94[ASN][1000 genomes]
rs1524774	0.85[YRI][hapmap]
rs1830006	0.94[ASN][1000 genomes]
rs1852010	0.80[AFR][1000 genomes]
rs1852011	0.80[AFR][1000 genomes]
rs1965534	0.96[ASN][1000 genomes]
rs1997019	0.94[ASN][1000 genomes]
rs2068172	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2110015	0.97[ASN][1000 genomes]
rs2254176	0.82[AFR][1000 genomes]
rs2254361	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2254594	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2254737	0.88[ASW][hapmap];0.87[CHB][hapmap];0.81[YRI][hapmap];0.85[ASN][1000 genomes]
rs2462512	0.81[YRI][hapmap]
rs2537592	1.00[ASN][1000 genomes]
rs2537593	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2537594	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691553	0.80[AFR][1000 genomes]
rs2691556	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691581	0.96[ASN][1000 genomes]
rs2691582	0.96[ASN][1000 genomes]
rs2691583	0.81[LWK][hapmap];0.82[MKK][hapmap];0.90[YRI][hapmap]
rs2691584	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691592	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691593	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691595	1.00[ASN][1000 genomes]
rs2691596	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691602	0.81[YRI][hapmap]
rs2691604	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691610	1.00[ASN][1000 genomes]
rs2691612	0.85[YRI][hapmap]
rs2691616	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691617	1.00[ASN][1000 genomes]
rs2691618	0.84[YRI][hapmap]
rs2691620	0.85[YRI][hapmap]
rs2691629	0.80[AFR][1000 genomes]
rs2691630	0.80[AFR][1000 genomes]
rs2723496	0.80[AFR][1000 genomes]
rs2723497	0.80[AFR][1000 genomes]
rs2723498	0.80[AFR][1000 genomes]
rs2723499	0.80[AFR][1000 genomes]
rs2723500	0.80[AFR][1000 genomes]
rs2723502	0.83[LWK][hapmap];0.81[YRI][hapmap]
rs2723503	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723506	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723507	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723508	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723509	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723511	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723513	1.00[ASN][1000 genomes]
rs2723514	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723516	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723517	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723518	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723519	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.85[MKK][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723520	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.92[MKK][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2723521	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2723540	0.81[YRI][hapmap]
rs2723571	0.81[YRI][hapmap]
rs4316058	0.93[CHB][hapmap];0.95[CHD][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs4721665	0.85[YRI][hapmap]
rs4721666	0.90[YRI][hapmap]
rs6973480	0.80[LWK][hapmap];0.85[YRI][hapmap]
rs949451	0.81[LWK][hapmap];0.94[MKK][hapmap];0.90[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869352	chr7:17237983-17932878	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1021524	chr7:17251148-17963307	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1021289	chr7:17254117-17873816	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv538754	chr7:17254117-17873816	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv534309	chr7:17254118-17932878	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv887804	chr7:17571140-17885468	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
9	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
10	esv1802979	chr7:17816528-17908546	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17812400-17846200	Weak transcription	Fetal Stomach	stomach
2	chr7:17812400-17852200	Weak transcription	Esophagus	oesophagus
3	chr7:17812600-17887600	Weak transcription	Gastric	stomach
4	chr7:17813400-17821200	Weak transcription	Thymus	Thymus
5	chr7:17813600-17879200	Weak transcription	HSMMtube	muscle
6	chr7:17813800-17833200	Weak transcription	Fetal Thymus	thymus
7	chr7:17813800-17836200	Weak transcription	HSMM	muscle
8	chr7:17814200-17833200	Weak transcription	Right Ventricle	heart
9	chr7:17814400-17821200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:17814600-17828600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:17814600-17833400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:17815000-17833200	Weak transcription	Left Ventricle	heart
13	chr7:17815200-17829200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:17815400-17821000	Weak transcription	NH-A	brain
15	chr7:17816200-17833200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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