Variant report

Variant	rs12064085
Chromosome Location	chr1:210050077-210050078
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10082248	1.00[CEU][hapmap]
rs10489343	1.00[AFR][1000 genomes]
rs10779514	1.00[AFR][1000 genomes]
rs10779515	1.00[AFR][1000 genomes]
rs10863789	1.00[AFR][1000 genomes]
rs10863790	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs1109430	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs11119347	1.00[AFR][1000 genomes]
rs11119348	1.00[AFR][1000 genomes]
rs11119359	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119360	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs12058100	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs12062600	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12063989	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12064211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12064398	1.00[AFR][1000 genomes]
rs12066340	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12069187	1.00[AFR][1000 genomes]
rs12075674	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs12078157	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12080691	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs12081405	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs12083685	1.00[CEU][hapmap]
rs12405750	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs12561766	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs12563527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12566152	1.00[AFR][1000 genomes]
rs13306422	1.00[AFR][1000 genomes]
rs17015078	1.00[CEU][hapmap]
rs17015217	1.00[CEU][hapmap]
rs17015255	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs17015268	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs1856161	1.00[AFR][1000 genomes]
rs1883332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2038053	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs2064163	0.80[ASN][1000 genomes]
rs2076149	1.00[AFR][1000 genomes]
rs2076151	1.00[AFR][1000 genomes]
rs2142860	1.00[AFR][1000 genomes]
rs2235371	1.00[AFR][1000 genomes]
rs2235377	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs2236902	1.00[CEU][hapmap]
rs2272866	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs2282740	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs2298930	1.00[CEU][hapmap]
rs3753517	1.00[AFR][1000 genomes]
rs41274836	1.00[AFR][1000 genomes]
rs4140636	1.00[CEU][hapmap]
rs4329516	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4545339	1.00[CEU][hapmap]
rs4844491	1.00[AFR][1000 genomes]
rs4844494	1.00[AFR][1000 genomes]
rs4844496	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4844498	0.98[AMR][1000 genomes]
rs4844893	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs4844894	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs4844908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57283682	1.00[AFR][1000 genomes]
rs6694238	1.00[CEU][hapmap]
rs7528642	1.00[CEU][hapmap]
rs846908	1.00[CEU][hapmap]
rs9919217	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv873139	chr1:209828955-210050794	Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210041000-210055400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:210045200-210051400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:210047400-210050200	Weak transcription	HUVEC	blood vessel
4	chr1:210047400-210051200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:210047400-210051200	Enhancers	HMEC	breast
6	chr1:210047400-210052600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:210047400-210053400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:210048800-210050600	Enhancers	Brain Cingulate Gyrus	brain
9	chr1:210048800-210050600	Enhancers	Fetal Brain Male	brain
10	chr1:210048800-210050800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:210048800-210050800	Enhancers	HSMMtube	muscle
12	chr1:210048800-210051800	Enhancers	Hela-S3	cervix
13	chr1:210049000-210050200	Enhancers	HSMM	muscle
14	chr1:210049000-210051200	Enhancers	NHDF-Ad	bronchial
15	chr1:210049200-210051000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:210049200-210051000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr1:210049200-210051000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:210049400-210050400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:210049400-210050600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr1:210049400-210051000	Enhancers	Brain Hippocampus Middle	brain
21	chr1:210049400-210052400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:210049400-210052400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:210049400-210052800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:210049400-210052800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:210049400-210056600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr1:210049600-210050200	Enhancers	Fetal Brain Female	brain
27	chr1:210049600-210050200	Enhancers	NH-A	brain
28	chr1:210049800-210050600	Enhancers	Brain Germinal Matrix	brain
29	chr1:210049800-210052200	Weak transcription	Brain Anterior Caudate	brain
30	chr1:210049800-210052200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr1:210049800-210052200	Weak transcription	Brain Substantia Nigra	brain
32	chr1:210049800-210052600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:210049800-210052800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:210050000-210051200	Enhancers	NHEK	skin
35	chr1:210050000-210052400	Weak transcription	Brain Angular Gyrus	brain
36	chr1:210050000-210052800	Weak transcription	Osteobl	bone

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