Variant report

Variant	rs11100724
Chromosome Location	chr4:142613269-142613270
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10028670	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1040257	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11100722	1.00[ASN][1000 genomes]
rs11100723	1.00[ASN][1000 genomes]
rs12508955	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13111860	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1476326	1.00[ASN][1000 genomes]
rs1493024	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1519552	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1519553	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1589241	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1607592	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1607593	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1850853	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2087849	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2254514	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2322262	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4956404	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4956407	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6537058	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6837991	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6841454	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6842194	1.00[ASN][1000 genomes]
rs7661408	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7688250	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7698675	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9683566	1.00[ASN][1000 genomes]
rs9684235	1.00[ASN][1000 genomes]
rs970327	1.00[ASN][1000 genomes]
rs970328	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs990851	0.89[EUR][1000 genomes];1.00[ASN][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	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1030822	chr4:142487721-142706053	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1027004	chr4:142487721-143007320	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	esv3448093	chr4:142612197-142704695	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv3448741	chr4:142612202-142614305	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142583400-142634600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:142601600-142613600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr4:142601800-142616400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr4:142602800-142616400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:142605800-142614600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:142608400-142628800	Weak transcription	Aorta	Aorta
7	chr4:142608400-142629000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:142608600-142615000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:142608800-142624200	Weak transcription	Spleen	Spleen
10	chr4:142608800-142655000	Weak transcription	Gastric	stomach
11	chr4:142612800-142613400	Enhancers	Left Ventricle	heart
12	chr4:142613000-142613800	Enhancers	Hela-S3	cervix
13	chr4:142613200-142613400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:142613200-142613400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:142613200-142613400	Enhancers	Esophagus	oesophagus
16	chr4:142613200-142613400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:142613200-142613600	Enhancers	A549	lung

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