Variant report

Variant	rs2076374
Chromosome Location	chr20:29875458-29875459
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	chr20:29874751..29877240-chr20:29903779..29906129,2	K562	blood:

Extended variants
information (count: 122 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1080568	0.96[ASN][1000 genomes]
rs13045866	0.92[ASN][1000 genomes]
rs1474945	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs1884743	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1980582	1.00[ASN][1000 genomes]
rs2076373	0.85[CHB][hapmap]
rs2076375	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143191	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2180566	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs2206381	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2206382	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.87[EUR][1000 genomes]
rs2206383	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.80[YRI][hapmap]
rs2223527	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap]
rs2233832	1.00[YRI][hapmap]
rs2273468	0.85[CHB][hapmap];0.85[CHD][hapmap]
rs2281554	1.00[CEU][hapmap];0.83[CHB][hapmap];0.92[YRI][hapmap];0.81[EUR][1000 genomes]
rs2295500	0.95[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap];0.80[ASN][1000 genomes]
rs2295501	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.91[YRI][hapmap];0.90[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2376538	0.94[ASN][1000 genomes]
rs2376858	0.83[CHB][hapmap]
rs35293804	0.94[ASN][1000 genomes]
rs3861819	1.00[YRI][hapmap]
rs4243975	0.93[ASN][1000 genomes]
rs4300919	0.95[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap]
rs4333000	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4525766	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4911191	0.99[ASN][1000 genomes]
rs4911211	0.89[ASN][1000 genomes]
rs4911274	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs4911306	0.84[CHB][hapmap]
rs4911329	1.00[CEU][hapmap];0.85[CHB][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];0.80[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.92[YRI][hapmap]
rs4911432	0.93[ASN][1000 genomes]
rs4911529	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4911530	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4911531	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4911555	0.94[ASN][1000 genomes]
rs4911557	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs5001275	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs6057649	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs6057704	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6057860	0.94[ASN][1000 genomes]
rs6057963	0.82[ASN][1000 genomes]
rs6058066	0.85[ASN][1000 genomes]
rs6058399	0.89[ASN][1000 genomes]
rs6058531	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs6058918	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs6059128	1.00[CEU][hapmap];0.83[CHB][hapmap];0.92[YRI][hapmap]
rs6059238	0.95[ASN][1000 genomes]
rs6059332	0.90[AMR][1000 genomes]
rs6059335	1.00[CEU][hapmap];0.85[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap];0.85[EUR][1000 genomes]
rs6059379	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs6059724	0.96[ASN][1000 genomes]
rs6059955	0.93[ASN][1000 genomes]
rs6059977	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6060006	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6060100	0.83[ASN][1000 genomes]
rs6061178	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs6061207	0.89[ASN][1000 genomes]
rs6061213	0.95[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs6087445	0.85[CHB][hapmap];0.93[CHD][hapmap];0.80[JPT][hapmap]
rs6087464	0.85[CHB][hapmap];0.87[CHD][hapmap]
rs6087468	0.85[CHB][hapmap];0.94[CHD][hapmap];0.80[JPT][hapmap]
rs6087777	0.99[ASN][1000 genomes]
rs6087831	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs6087852	0.90[ASN][1000 genomes]
rs6087854	0.89[ASN][1000 genomes]
rs6087927	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6088036	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs6088076	0.86[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6088077	0.80[ASN][1000 genomes]
rs6088109	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];0.80[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs6088112	0.85[CHB][hapmap];0.80[JPT][hapmap]
rs6088144	0.85[CHB][hapmap];0.80[JPT][hapmap]
rs6088167	0.90[ASN][1000 genomes]
rs6088215	1.00[CEU][hapmap];0.85[CHB][hapmap];0.90[CHD][hapmap];0.88[GIH][hapmap];0.80[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap]
rs6088264	0.90[ASN][1000 genomes]
rs6088591	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6088748	0.97[ASN][1000 genomes]
rs6089126	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs6120006	0.95[ASN][1000 genomes]
rs6120575	0.97[ASN][1000 genomes]
rs6141536	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6141934	0.85[CHB][hapmap];0.80[JPT][hapmap]
rs6142150	0.93[ASN][1000 genomes]
rs6142220	0.93[ASN][1000 genomes]
rs6142241	0.96[ASN][1000 genomes]
rs709045	0.95[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap];0.80[ASN][1000 genomes]
rs732861	0.98[ASN][1000 genomes]
rs734418	0.85[CHB][hapmap];0.93[CHD][hapmap]
rs760996	1.00[CEU][hapmap];0.85[CHB][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap]
rs8183998	0.84[ASN][1000 genomes]
rs975075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9798579	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869384	chr20:29833386-30605088	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	419 gene(s)	inside rSNPs	diseases
2	nsv833951	chr20:29833448-29878205	Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv458960	chr20:29833609-29912852	Active TSS ZNF genes & repeats Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv585909	chr20:29833609-29912852	Active TSS Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv470546	chr20:29833609-30235302	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	385 gene(s)	inside rSNPs	diseases
6	nsv1065124	chr20:29833958-29912341	Active TSS ZNF genes & repeats Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv544227	chr20:29833958-29912341	ZNF genes & repeats Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1061669	chr20:29833958-29926862	Active TSS ZNF genes & repeats Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1066609	chr20:29833958-29938132	ZNF genes & repeats Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv544228	chr20:29833958-29938132	ZNF genes & repeats Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1066779	chr20:29833958-29981427	ZNF genes & repeats Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv544229	chr20:29833958-29981427	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv1060567	chr20:29833958-29992219	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv544230	chr20:29833958-29992219	ZNF genes & repeats Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
15	nsv1059642	chr20:29833958-30024839	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv544231	chr20:29833958-30024839	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	nsv1055527	chr20:29833958-30078925	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
18	nsv1062069	chr20:29833958-30153486	Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
19	nsv1062612	chr20:29833958-30219337	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	383 gene(s)	inside rSNPs	diseases
20	nsv1061673	chr20:29833958-30649496	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
21	nsv544232	chr20:29833958-30649496	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
22	nsv1063413	chr20:29835037-29969913	ZNF genes & repeats Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
23	nsv1065102	chr20:29835037-30011213	ZNF genes & repeats Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv1058516	chr20:29835037-30024168	ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
25	nsv1058344	chr20:29835037-30386611	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	402 gene(s)	inside rSNPs	diseases
26	nsv1059672	chr20:29835037-30621271	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	419 gene(s)	inside rSNPs	diseases
27	esv2763228	chr20:29835049-30239522	Genic enhancers Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	385 gene(s)	inside rSNPs	diseases
28	nsv949085	chr20:29846303-30473188	Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	414 gene(s)	inside rSNPs	diseases
29	nsv1060247	chr20:29860167-29969913	ZNF genes & repeats Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2076374	MRPL11	trans	parietal	SCAN
rs2076374	COX4I2	cis	parietal	SCAN
rs2076374	C20orf134	cis	cerebellum	SCAN
rs2076374	GFM2	trans	parietal	SCAN

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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