Variant report

Variant	rs8176583
Chromosome Location	chr2:188334401-188334402
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:188332292..188334574-chr2:188338658..188340896,2	K562	blood:

Extended variants
information (count: 175 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:152)

rs_ID	r²[population]
rs10174456	0.90[ASN][1000 genomes]
rs10174735	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10179705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10181823	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10181845	0.81[ASN][1000 genomes]
rs10191833	0.81[ASN][1000 genomes]
rs10194145	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10194247	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10201618	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10203398	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10203781	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10931283	0.88[CEU][hapmap]
rs10931284	0.84[CEU][hapmap]
rs10931288	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10931289	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11674362	0.87[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap]
rs11685426	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11689123	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691442	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11894589	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11897572	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11903296	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12104503	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap]
rs12693471	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12987470	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13019491	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13024536	0.89[ASN][1000 genomes]
rs13028645	0.91[ASN][1000 genomes]
rs13392310	0.84[ASN][1000 genomes]
rs13408875	0.84[CHD][hapmap]
rs13409829	0.87[ASN][1000 genomes]
rs13411274	0.92[CEU][hapmap]
rs13418253	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13424790	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13425233	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13430354	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13430665	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1355519	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1355520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1398061	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1528233	0.90[ASN][1000 genomes]
rs1528236	0.81[ASN][1000 genomes]
rs1609268	0.90[ASN][1000 genomes]
rs1632282	0.90[ASN][1000 genomes]
rs16829016	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1706261	0.90[ASN][1000 genomes]
rs1706262	0.90[ASN][1000 genomes]
rs1706273	0.81[ASN][1000 genomes]
rs1706276	0.90[ASN][1000 genomes]
rs1728678	0.81[ASN][1000 genomes]
rs1728680	0.90[ASN][1000 genomes]
rs1728690	0.90[ASN][1000 genomes]
rs17367055	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17464221	0.89[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.97[ASN][1000 genomes]
rs17756804	0.81[ASN][1000 genomes]
rs1912846	0.82[ASN][1000 genomes]
rs1912847	0.82[ASN][1000 genomes]
rs1912848	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1983492	0.92[ASN][1000 genomes]
rs2030976	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2041778	0.84[CHD][hapmap]
rs2058670	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2349315	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2882203	1.00[CHB][hapmap]
rs35056802	0.91[ASN][1000 genomes]
rs35721125	0.81[ASN][1000 genomes]
rs35870933	0.91[ASN][1000 genomes]
rs36110670	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36146505	0.92[ASN][1000 genomes]
rs3755248	0.84[CHD][hapmap]
rs3771058	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3771059	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3771061	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3771067	0.83[CEU][hapmap];0.88[CHB][hapmap];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3771076	1.00[CHB][hapmap]
rs3771078	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3821180	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3821184	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4140885	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4667160	0.81[ASN][1000 genomes]
rs59400383	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6434219	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6719550	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67285003	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6744012	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6753700	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs696092	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs698579	0.92[CEU][hapmap];0.81[CHB][hapmap];0.83[CHD][hapmap];0.92[ASN][1000 genomes]
rs698582	0.92[ASN][1000 genomes]
rs698583	0.92[ASN][1000 genomes]
rs698588	0.92[ASN][1000 genomes]
rs698590	0.92[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs698592	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs698593	0.89[ASN][1000 genomes]
rs72902495	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7576066	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7586970	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7589163	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7591567	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7598858	0.94[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8176472	0.84[ASN][1000 genomes]
rs8176479	0.90[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs8176498	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8176501	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8176506	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8176525	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8176526	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8176528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8176541	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8176546	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8176547	0.82[ASN][1000 genomes]
rs8176548	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[ASN][1000 genomes]
rs8176580	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8176592	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs840564	0.81[ASN][1000 genomes]
rs840567	0.81[ASN][1000 genomes]
rs840569	0.81[ASN][1000 genomes]
rs840570	0.81[ASN][1000 genomes]
rs840571	0.81[ASN][1000 genomes]
rs840572	0.81[ASN][1000 genomes]
rs840574	0.81[ASN][1000 genomes]
rs840576	0.81[ASN][1000 genomes]
rs840577	0.81[ASN][1000 genomes]
rs840578	0.81[ASN][1000 genomes]
rs840583	0.87[ASN][1000 genomes]
rs840584	0.87[ASN][1000 genomes]
rs840585	0.87[ASN][1000 genomes]
rs840586	0.87[ASN][1000 genomes]
rs840587	0.87[ASN][1000 genomes]
rs840588	0.87[ASN][1000 genomes]
rs840589	0.87[ASN][1000 genomes]
rs840590	0.87[ASN][1000 genomes]
rs840591	0.86[ASN][1000 genomes]
rs840593	0.87[ASN][1000 genomes]
rs840595	0.87[ASN][1000 genomes]
rs840596	0.87[ASN][1000 genomes]
rs840597	0.87[ASN][1000 genomes]
rs840609	0.90[ASN][1000 genomes]
rs840610	0.90[ASN][1000 genomes]
rs840611	0.90[ASN][1000 genomes]
rs840616	0.90[ASN][1000 genomes]
rs858744	0.88[CEU][hapmap];0.90[CHB][hapmap];0.87[CHD][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs858756	0.92[ASN][1000 genomes]
rs858758	0.93[ASN][1000 genomes]
rs858759	0.87[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs860846	0.92[ASN][1000 genomes]
rs860859	0.90[ASN][1000 genomes]
rs863972	0.90[ASN][1000 genomes]
rs865763	0.81[ASN][1000 genomes]
rs880890	0.87[ASN][1000 genomes]
rs907463	0.87[ASN][1000 genomes]
rs9288140	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949700	chr2:187713412-188361211	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv834487	chr2:188182556-188353363	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv875557	chr2:188219052-188370232	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv875558	chr2:188219052-188388311	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv875559	chr2:188219052-188390112	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv875560	chr2:188219052-188508011	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv875561	chr2:188226900-188440752	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv584036	chr2:188256158-188369841	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv875562	chr2:188258904-188370232	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv875563	chr2:188258904-188388311	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
11	nsv875564	chr2:188258904-188414161	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
12	nsv875565	chr2:188258904-188440752	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
13	nsv875566	chr2:188258904-188626214	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	nsv875567	chr2:188258904-188673462	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
15	nsv834488	chr2:188268434-188415496	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
16	nsv875568	chr2:188291105-188653806	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv1011800	chr2:188301324-188340396	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
18	nsv875569	chr2:188327904-188341047	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
19	nsv875570	chr2:188330682-188340335	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
20	nsv875571	chr2:188330682-188341047	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
21	nsv875572	chr2:188330682-188355835	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
22	nsv875573	chr2:188331704-188343131	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv875574	chr2:188333064-188341047	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs8176583	CALCRL	cis	Artery Tibial	GTEx
rs8176583	CALCRL	cis	multi-tissue	Pritchard

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188313400-188340000	Weak transcription	Fetal Brain Male	brain
2	chr2:188326800-188341800	Weak transcription	Adipose Nuclei	Adipose
3	chr2:188326800-188353600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr2:188326800-188357600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:188326800-188357800	Weak transcription	Lung	lung
6	chr2:188327000-188337400	Weak transcription	Pancreas	Pancrea
7	chr2:188327000-188339200	Weak transcription	Fetal Intestine Small	intestine
8	chr2:188327000-188357800	Weak transcription	Left Ventricle	heart
9	chr2:188327200-188357600	Weak transcription	Fetal Intestine Large	intestine
10	chr2:188327400-188339000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:188327600-188341200	Weak transcription	NHDF-Ad	bronchial
12	chr2:188328200-188342200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr2:188328200-188357600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:188328200-188360000	Weak transcription	Psoas Muscle	Psoas
15	chr2:188328400-188341800	Weak transcription	NHLF	lung
16	chr2:188328400-188343400	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:188328400-188365400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:188328600-188357200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr2:188328800-188342000	Weak transcription	HSMMtube	muscle
20	chr2:188328800-188343000	Weak transcription	Fetal Stomach	stomach
21	chr2:188329000-188341800	Strong transcription	HSMM	muscle
22	chr2:188329000-188358000	Weak transcription	K562	blood
23	chr2:188329200-188340200	Weak transcription	Hela-S3	cervix
24	chr2:188329200-188347800	Strong transcription	Liver	Liver
25	chr2:188329800-188338600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr2:188330200-188337400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr2:188330600-188344400	Weak transcription	Fetal Lung	lung
28	chr2:188330800-188335200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:188331200-188334800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:188331200-188336200	Strong transcription	HepG2	liver
31	chr2:188332000-188340200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:188332400-188336000	Strong transcription	HUVEC	blood vessel
33	chr2:188332800-188357600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr2:188333000-188335200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:188333000-188337000	Weak transcription	Aorta	Aorta
36	chr2:188333200-188334800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:188333600-188334800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr2:188333600-188335000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:188333600-188337200	Weak transcription	Placenta	Placenta
40	chr2:188333600-188337400	Weak transcription	Osteobl	bone
41	chr2:188333600-188341200	Weak transcription	NH-A	brain
42	chr2:188333800-188335000	Weak transcription	NHEK	skin
43	chr2:188334000-188334800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:188334000-188339600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr2:188334200-188335600	Strong transcription	Primary hematopoietic stem cells	blood
46	chr2:188334200-188336000	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr2:188334200-188374600	Weak transcription	Placenta Amnion	Placenta Amnion

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