Variant report

Variant	rs2736288
Chromosome Location	chr8:11228100-11228101
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:11221017..11222981-chr8:11226248..11228543,2	K562	blood:
2	chr8:11224632..11226461-chr8:11227534..11229190,2	K562	blood:
3	chr8:11200246..11202306-chr8:11227732..11229716,2	K562	blood:

Variant related genes	Relation type
ENSG00000184608	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1047950	0.86[CEU][hapmap]
rs10503421	0.82[AMR][1000 genomes]
rs11250130	0.92[CEU][hapmap]
rs11781637	0.92[CEU][hapmap]
rs11782430	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12547100	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12549871	0.82[AMR][1000 genomes]
rs12550129	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12682349	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13260727	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13268126	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13269118	0.85[ASN][1000 genomes]
rs13274106	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1435274	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1435275	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1435277	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs1560971	0.85[ASN][1000 genomes]
rs1865521	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2043508	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2043510	0.86[AMR][1000 genomes]
rs2246606	0.89[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2249804	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2250028	0.92[CEU][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2263511	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2263512	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2409756	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2437152	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2572371	0.83[AMR][1000 genomes]
rs2572379	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2572380	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2572382	0.90[CEU][hapmap];0.82[AMR][1000 genomes]
rs2572385	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs2572386	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2572389	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2572391	0.87[AMR][1000 genomes]
rs2572394	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2572395	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2572399	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2572400	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2572440	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2572450	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2572452	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2736270	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs2736278	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2736282	0.85[AMR][1000 genomes]
rs2736283	0.86[AMR][1000 genomes]
rs2736285	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736286	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2736287	0.86[AMR][1000 genomes]
rs2736290	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736292	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2736293	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736294	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736295	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736296	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736297	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736298	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736300	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2736302	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2736303	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2736304	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2898272	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34389419	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34482136	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34964435	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35009431	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4363158	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4448232	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4631424	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4841524	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4841525	0.85[ASN][1000 genomes]
rs55758514	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56177149	0.85[ASN][1000 genomes]
rs57629785	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6601582	0.83[CEU][hapmap]
rs6601584	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6601585	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7820301	0.87[AMR][1000 genomes]
rs7821302	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7821459	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7828263	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7834572	0.94[AMR][1000 genomes];0.93[EUR][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	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv831233	chr8:11046854-11234384	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised 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 miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1033312	chr8:11126800-11252170	Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv890354	chr8:11176147-11266131	Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2736288	C8orf5	Cis_1M	lymphoblastoid	RTeQTL
rs2736288	BLK	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11218000-11237600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:11223400-11229000	Weak transcription	Pancreas	Pancrea
3	chr8:11225400-11229800	Weak transcription	K562	blood

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