Variant report

Variant	rs8033734
Chromosome Location	chr15:42663583-42663584
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12441027	1.00[MEX][hapmap]
rs1678998	1.00[MEX][hapmap]
rs16972927	0.83[EUR][1000 genomes]
rs16972930	0.83[EUR][1000 genomes]
rs16972969	0.83[EUR][1000 genomes]
rs16973015	1.00[GIH][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs16973018	0.83[EUR][1000 genomes]
rs16973022	0.83[EUR][1000 genomes]
rs16973177	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973182	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973184	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973188	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973200	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16973206	1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973233	1.00[MEX][hapmap]
rs17593	1.00[ASW][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2412694	1.00[MEX][hapmap]
rs2412697	1.00[MEX][hapmap]
rs28364383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28364385	0.89[AFR][1000 genomes]
rs28364387	0.83[EUR][1000 genomes]
rs28364395	1.00[MEX][hapmap]
rs28364396	1.00[MEX][hapmap]
rs28364399	0.87[ASW][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28364407	1.00[MEX][hapmap]
rs28364423	1.00[GIH][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs28364432	1.00[MEX][hapmap]
rs28364443	1.00[MEX][hapmap]
rs28364485	1.00[MEX][hapmap]
rs28364496	1.00[MEX][hapmap]
rs28364534	1.00[MEX][hapmap]
rs4307925	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4486855	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4516202	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4923941	1.00[MEX][hapmap]
rs4924650	1.00[MEX][hapmap]
rs4924668	1.00[MEX][hapmap]
rs4924669	1.00[MEX][hapmap]
rs4924671	1.00[MEX][hapmap]
rs5029919	0.86[EUR][1000 genomes]
rs7167683	1.00[ASW][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7174880	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7176832	1.00[MEX][hapmap]
rs728507	1.00[EUR][1000 genomes]
rs728508	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs728509	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs728510	0.83[EUR][1000 genomes]
rs8024452	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8026890	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8027800	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8033108	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8033882	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8033960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8035332	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8035521	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8037627	1.00[MEX][hapmap]
rs8038771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8038967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8039470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8040129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8040726	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs934877	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv904133	chr15:42528982-42681057	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv832986	chr15:42587825-42753664	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv832987	chr15:42627447-42792348	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv932995	chr15:42640015-42704121	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42645600-42663600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr15:42645600-42677800	Weak transcription	Spleen	Spleen
3	chr15:42646000-42678600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:42647800-42678200	Weak transcription	Ovary	ovary
5	chr15:42649800-42673200	Weak transcription	Thymus	Thymus
6	chr15:42650800-42664000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr15:42652400-42665400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:42652800-42684400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr15:42653200-42691600	Weak transcription	Stomach Smooth Muscle	stomach
10	chr15:42654200-42677800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr15:42654400-42665400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:42654800-42669400	Weak transcription	Liver	Liver
13	chr15:42656000-42678800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:42656800-42663600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr15:42656800-42693400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:42656800-42697800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:42657000-42665600	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:42657000-42665600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr15:42657200-42665800	Weak transcription	Left Ventricle	heart
20	chr15:42657200-42678800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr15:42659600-42676800	Weak transcription	Lung	lung
22	chr15:42660200-42663600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr15:42660200-42663800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr15:42661400-42665400	Weak transcription	Fetal Muscle Leg	muscle
25	chr15:42662000-42664600	Weak transcription	Psoas Muscle	Psoas
26	chr15:42662400-42663600	Enhancers	HepG2	liver
27	chr15:42663000-42665600	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr15:42663000-42691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:42663200-42664400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:42663200-42669400	Weak transcription	Primary B cells from cord blood	blood
31	chr15:42663200-42678400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:42663400-42663800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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