Variant report

Variant	rs2723513
Chromosome Location	chr7:17814888-17814889
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-11	chr7:17812631-17814939	NONHSAT119344

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10249221	0.91[ASN][1000 genomes]
rs10264355	1.00[ASN][1000 genomes]
rs10264445	0.91[ASN][1000 genomes]
rs10264447	0.91[ASN][1000 genomes]
rs1404416	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1404417	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404418	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404419	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404421	0.99[ASN][1000 genomes]
rs1404425	0.94[ASN][1000 genomes]
rs1830006	0.94[ASN][1000 genomes]
rs1965534	0.96[ASN][1000 genomes]
rs1997019	0.94[ASN][1000 genomes]
rs2068172	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110015	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2254361	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2254594	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2254737	0.86[CHB][hapmap];0.85[ASN][1000 genomes]
rs2537592	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537593	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537594	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691555	0.81[YRI][hapmap]
rs2691556	1.00[ASN][1000 genomes]
rs2691559	0.88[YRI][hapmap]
rs2691581	0.96[ASN][1000 genomes]
rs2691582	0.96[ASN][1000 genomes]
rs2691584	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2691592	1.00[ASN][1000 genomes]
rs2691593	1.00[ASN][1000 genomes]
rs2691595	1.00[ASN][1000 genomes]
rs2691596	1.00[ASN][1000 genomes]
rs2691604	1.00[ASN][1000 genomes]
rs2691610	1.00[ASN][1000 genomes]
rs2691616	1.00[ASN][1000 genomes]
rs2691617	1.00[ASN][1000 genomes]
rs2691621	0.82[AFR][1000 genomes]
rs2691627	0.82[AFR][1000 genomes]
rs2691628	0.86[AFR][1000 genomes]
rs2723503	1.00[ASN][1000 genomes]
rs2723506	1.00[ASN][1000 genomes]
rs2723507	1.00[ASN][1000 genomes]
rs2723508	1.00[ASN][1000 genomes]
rs2723509	1.00[ASN][1000 genomes]
rs2723510	1.00[ASN][1000 genomes]
rs2723511	1.00[ASN][1000 genomes]
rs2723514	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723515	0.81[YRI][hapmap]
rs2723516	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723517	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723518	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723519	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2723521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4316058	0.93[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]

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	esv2764016	chr7:17800816-17815402	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17810200-17815000	Enhancers	HMEC	breast
2	chr7:17812000-17815000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:17812000-17815200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:17812200-17815200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:17812200-17815400	Enhancers	NH-A	brain
6	chr7:17812400-17815000	Enhancers	Osteobl	bone
7	chr7:17812400-17846200	Weak transcription	Fetal Stomach	stomach
8	chr7:17812400-17852200	Weak transcription	Esophagus	oesophagus
9	chr7:17812600-17887600	Weak transcription	Gastric	stomach
10	chr7:17813000-17815000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:17813400-17815000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:17813400-17821200	Weak transcription	Thymus	Thymus
13	chr7:17813600-17879200	Weak transcription	HSMMtube	muscle
14	chr7:17813800-17815400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr7:17813800-17833200	Weak transcription	Fetal Thymus	thymus
16	chr7:17813800-17836200	Weak transcription	HSMM	muscle
17	chr7:17814200-17833200	Weak transcription	Right Ventricle	heart
18	chr7:17814400-17815600	Enhancers	Fetal Heart	heart
19	chr7:17814400-17821200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:17814600-17828600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:17814600-17833400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:17814800-17815000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:17814800-17815000	Enhancers	Placenta	Placenta
24	chr7:17814800-17815000	Enhancers	Left Ventricle	heart

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