Variant report

Variant	rs2367555
Chromosome Location	chr4:75119001-75119002
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10009707	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10013212	0.88[EUR][1000 genomes]
rs10017409	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10017417	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10018373	0.90[EUR][1000 genomes]
rs10019396	0.87[EUR][1000 genomes]
rs10023519	0.81[EUR][1000 genomes]
rs10026687	0.81[EUR][1000 genomes]
rs10028285	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1037824	0.88[EUR][1000 genomes]
rs10433673	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10938112	0.87[EUR][1000 genomes]
rs11724468	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11737662	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11945418	0.81[EUR][1000 genomes]
rs1246575	0.88[EUR][1000 genomes]
rs1246577	0.90[EUR][1000 genomes]
rs1246578	0.87[EUR][1000 genomes]
rs1246579	0.87[EUR][1000 genomes]
rs1246580	0.86[EUR][1000 genomes]
rs1246582	0.90[EUR][1000 genomes]
rs1246584	0.90[EUR][1000 genomes]
rs1246586	0.90[EUR][1000 genomes]
rs1246587	0.90[EUR][1000 genomes]
rs1246588	0.90[EUR][1000 genomes]
rs1246590	0.87[EUR][1000 genomes]
rs1246591	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1246594	0.84[EUR][1000 genomes]
rs1246597	0.86[EUR][1000 genomes]
rs12500697	0.86[EUR][1000 genomes]
rs1265327	0.90[EUR][1000 genomes]
rs13116896	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13142241	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1371796	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1371797	0.84[EUR][1000 genomes]
rs1380561	0.93[EUR][1000 genomes]
rs1460016	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1460017	0.86[EUR][1000 genomes]
rs16850862	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16850883	0.88[EUR][1000 genomes]
rs17232394	0.81[EUR][1000 genomes]
rs1964526	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2045616	0.88[EUR][1000 genomes]
rs2045617	0.88[EUR][1000 genomes]
rs2045618	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2061508	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2367745	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28378517	0.85[EUR][1000 genomes]
rs28436705	0.88[EUR][1000 genomes]
rs28539097	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28644493	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28695994	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4371587	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4502653	0.81[EUR][1000 genomes]
rs4577545	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4694184	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs488440	0.87[EUR][1000 genomes]
rs536541	0.84[EUR][1000 genomes]
rs565831	0.84[EUR][1000 genomes]
rs58813617	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62312513	0.89[EUR][1000 genomes]
rs62312515	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62312545	0.82[EUR][1000 genomes]
rs6446983	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6446984	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6446985	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6811214	0.82[EUR][1000 genomes]
rs6814880	0.88[EUR][1000 genomes]
rs6819605	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6820992	0.88[EUR][1000 genomes]
rs6821664	0.82[EUR][1000 genomes]
rs6835734	0.87[EUR][1000 genomes]
rs6854203	0.93[EUR][1000 genomes]
rs6854723	0.82[EUR][1000 genomes]
rs7659389	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7663269	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7665105	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7670535	0.82[EUR][1000 genomes]
rs7672588	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7676371	0.84[EUR][1000 genomes]
rs7678292	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7681137	0.84[EUR][1000 genomes]
rs7681763	0.84[EUR][1000 genomes]
rs7681912	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7683181	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9992393	0.93[EUR][1000 genomes]
rs9997322	0.82[EUR][1000 genomes]
rs9997788	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1013260	chr4:75013441-75121643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002907	chr4:75013441-75131443	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1004706	chr4:75014770-75121643	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1009099	chr4:75089233-75726206	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75114800-75119200	Weak transcription	Pancreas	Pancrea
2	chr4:75115800-75120000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:75116400-75120000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
4	chr4:75117400-75119200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:75117400-75120000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr4:75117600-75119800	ZNF genes & repeats	NHEK	skin
7	chr4:75117800-75119200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:75118000-75119200	Weak transcription	Right Ventricle	heart
9	chr4:75118200-75119200	Weak transcription	Aorta	Aorta
10	chr4:75119000-75119600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
11	chr4:75119000-75119800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:75119000-75119800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr4:75119000-75120000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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