Variant report

Variant	rs3804162
Chromosome Location	chr4:121697932-121697933
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10518379	0.83[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs11726349	0.83[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs11728387	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11733915	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs11734461	0.81[CHB][hapmap];0.84[JPT][hapmap];0.83[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs11735169	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12499000	0.94[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[MKK][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12500166	0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12502113	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12504122	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12507359	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12507922	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12507924	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12507970	0.88[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs12508015	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12508048	0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12508821	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12509870	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12509912	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12509939	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12509993	0.85[CHB][hapmap];0.92[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1511303	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1511304	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1511305	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1511307	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1511308	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1567551	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs17051248	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs17051250	0.96[ASN][1000 genomes]
rs17051251	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs17051256	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs17051258	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs17051260	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs17051266	0.83[CHB][hapmap];0.90[JPT][hapmap];0.83[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1949110	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1949111	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2122510	0.81[JPT][hapmap]
rs2203059	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2203060	0.94[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[MKK][hapmap];0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2221813	0.89[ASN][1000 genomes]
rs2221814	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2221815	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs34151748	0.92[ASN][1000 genomes]
rs3761721	0.94[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs3804163	0.97[ASN][1000 genomes]
rs3804164	0.97[ASN][1000 genomes]
rs3804165	0.97[ASN][1000 genomes]
rs3804166	0.97[ASN][1000 genomes]
rs3804167	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs3804168	0.96[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs3804169	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs3804171	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs3827583	0.97[ASN][1000 genomes]
rs4336252	0.86[CHB][hapmap];0.86[JPT][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs4833178	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4833179	0.94[CHB][hapmap];0.96[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[MKK][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4833180	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4833181	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4833186	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4833674	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4833680	0.88[CHB][hapmap];0.96[CHD][hapmap];0.90[GIH][hapmap];0.87[JPT][hapmap];1.00[MKK][hapmap];0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4833684	0.84[ASN][1000 genomes]
rs4833686	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4833687	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs55901892	0.97[ASN][1000 genomes]
rs56402218	0.97[ASN][1000 genomes]
rs6534216	0.83[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs6811794	0.93[JPT][hapmap]
rs72921534	0.97[ASN][1000 genomes]
rs729934	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7377202	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1004485	chr4:121542992-121716769	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv916737	chr4:121589793-121748847	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv461634	chr4:121623057-121765527	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv595334	chr4:121623057-121765527	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1013704	chr4:121657648-121791601	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
8	nsv879855	chr4:121691899-121747335	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
9	nsv879856	chr4:121697932-121737767	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
10	nsv879857	chr4:121697932-121747335	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121671800-121728600	Weak transcription	Left Ventricle	heart
2	chr4:121672000-121722400	Weak transcription	Right Ventricle	heart
3	chr4:121672400-121728800	Weak transcription	Aorta	Aorta
4	chr4:121672400-121728800	Weak transcription	Fetal Stomach	stomach
5	chr4:121673000-121705200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:121673000-121722400	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:121673000-121737400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:121677000-121702800	Weak transcription	Gastric	stomach
9	chr4:121677000-121707800	Weak transcription	Psoas Muscle	Psoas
10	chr4:121677200-121714000	Weak transcription	Fetal Intestine Large	intestine
11	chr4:121677200-121723400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:121679600-121721800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:121686000-121705200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:121689800-121703000	Weak transcription	Brain Angular Gyrus	brain
15	chr4:121690600-121715800	Weak transcription	Lung	lung
16	chr4:121690600-121719600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:121690600-121728800	Weak transcription	Fetal Intestine Small	intestine
18	chr4:121691200-121705400	Weak transcription	HSMM	muscle
19	chr4:121691200-121722200	Weak transcription	Ovary	ovary
20	chr4:121693400-121698000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr4:121693400-121703600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr4:121695800-121730000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr4:121696400-121698200	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr4:121697000-121698200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr4:121697200-121706200	Weak transcription	Pancreas	Pancrea
26	chr4:121697800-121699200	Enhancers	Fetal Lung	lung

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