Variant report

Variant	rs73346620
Chromosome Location	chr6:2407684-2407685
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	chr6:2406407..2408708-chr6:2411442..2413753,3	K562	blood:
2	chr6:2406407..2408708-chr6:2411447..2413753,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WRNIP1-2	chr6:2403917-2409577	NONHSAT106665

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10155673	0.89[AMR][1000 genomes]
rs10155682	0.89[AMR][1000 genomes]
rs10155748	0.89[AMR][1000 genomes]
rs11964241	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11964259	0.89[AMR][1000 genomes]
rs11964680	0.89[AMR][1000 genomes]
rs28633763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34500504	0.89[AMR][1000 genomes]
rs4602753	0.87[AMR][1000 genomes]
rs56714114	0.89[AMR][1000 genomes]
rs57504362	0.89[AMR][1000 genomes]
rs57908018	0.87[AMR][1000 genomes]
rs59455919	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59920917	0.87[AMR][1000 genomes]
rs60798809	0.87[AMR][1000 genomes]
rs6901457	0.87[AMR][1000 genomes]
rs6904942	0.87[AMR][1000 genomes]
rs6905100	0.87[AMR][1000 genomes]
rs6905118	0.87[AMR][1000 genomes]
rs6909863	0.87[AMR][1000 genomes]
rs6925879	0.89[AMR][1000 genomes]
rs6929207	0.87[AMR][1000 genomes]
rs73344747	0.87[AMR][1000 genomes]
rs73344778	1.00[AMR][1000 genomes]
rs73344794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73344796	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73344799	0.89[AMR][1000 genomes]
rs73346609	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73346610	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73346662	0.87[AMR][1000 genomes]
rs73346668	0.87[AMR][1000 genomes]
rs73346669	0.87[AMR][1000 genomes]
rs73346702	0.87[AMR][1000 genomes]
rs73348609	0.87[AMR][1000 genomes]
rs7739140	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7744661	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9501832	0.89[AMR][1000 genomes]
rs9501833	0.89[AMR][1000 genomes]
rs9501834	0.89[AMR][1000 genomes]
rs9501835	0.89[AMR][1000 genomes]
rs9503154	0.87[AMR][1000 genomes]
rs9503156	0.87[AMR][1000 genomes]
rs9503165	0.87[AMR][1000 genomes]
rs9503170	0.89[AMR][1000 genomes]
rs9503171	0.89[AMR][1000 genomes]
rs9503172	0.89[AMR][1000 genomes]
rs9503173	0.89[AMR][1000 genomes]
rs9503174	0.89[AMR][1000 genomes]
rs9503177	0.89[AMR][1000 genomes]
rs9503178	0.89[AMR][1000 genomes]
rs9503179	0.89[AMR][1000 genomes]
rs9503181	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
2	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
3	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv1021573	chr6:2246721-2832408	Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
5	nsv538102	chr6:2246721-2832408	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
6	nsv883390	chr6:2265344-2584919	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv883391	chr6:2282747-2507448	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1016878	chr6:2375784-2680476	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv498004	chr6:2380300-3313587	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	163 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2392400-2414400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:2396800-2415400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:2397000-2409400	Weak transcription	HepG2	liver
4	chr6:2397200-2410200	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:2398000-2412600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:2399800-2409000	Weak transcription	Thymus	Thymus
7	chr6:2399800-2414000	Weak transcription	Fetal Stomach	stomach
8	chr6:2399800-2449200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:2401200-2417400	Weak transcription	Pancreas	Pancrea
10	chr6:2401200-2421000	Weak transcription	Fetal Intestine Large	intestine
11	chr6:2401400-2413000	Weak transcription	Adipose Nuclei	Adipose
12	chr6:2401400-2414000	Weak transcription	Lung	lung
13	chr6:2401400-2426200	Weak transcription	Aorta	Aorta
14	chr6:2401600-2413800	Weak transcription	Fetal Intestine Small	intestine
15	chr6:2402000-2407800	Weak transcription	Fetal Lung	lung
16	chr6:2402000-2415600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr6:2402200-2417400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:2402200-2449200	Weak transcription	Left Ventricle	heart
19	chr6:2404000-2415200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:2404400-2415400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:2404800-2414000	Weak transcription	Liver	Liver
22	chr6:2405000-2417800	Weak transcription	Primary T cells from cord blood	blood
23	chr6:2406200-2411000	Weak transcription	Ovary	ovary

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