Variant report

Variant	rs3787925
Chromosome Location	chr21:40826305-40826306
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:40825413..40827744-chr21:40969940..40971698,2	MCF-7	breast:
2	chr21:40821968..40825719-chr21:40825995..40830907,7	K562	blood:
3	chr21:40759594..40762847-chr21:40823318..40826677,3	K562	blood:
4	chr21:40820536..40825890-chr21:40826084..40828688,4	K562	blood:
5	chr21:40825465..40827848-chr21:40854649..40856447,2	K562	blood:

Variant related genes	Relation type
ENSG00000182093	Chromatin interaction
ENSG00000185437	Chromatin interaction
ENSG00000184809	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11088476	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1722873	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1735136	0.84[CHB][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1735137	0.82[CHB][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2063999	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2277788	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2410157	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2837003	0.81[JPT][hapmap]
rs2837004	0.81[JPT][hapmap]
rs3827209	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4358205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4389391	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4608607	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4818037	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6517551	0.84[CHB][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6517552	0.82[CHB][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7277386	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs760284	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8127431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8129943	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8130752	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9680225	0.90[EUR][1000 genomes]
rs975479	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs975934	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9979083	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9982529	0.82[CHB][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059868	chr21:40711535-41043291	Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40822800-40828600	Active TSS	Right Ventricle	heart
2	chr21:40824000-40852400	Weak transcription	Pancreas	Pancrea
3	chr21:40824600-40826800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr21:40824800-40828000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr21:40824800-40828400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr21:40825000-40847800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr21:40825200-40826400	Weak transcription	Left Ventricle	heart
8	chr21:40825200-40828400	Enhancers	Brain Cingulate Gyrus	brain
9	chr21:40825400-40826400	Weak transcription	Psoas Muscle	Psoas
10	chr21:40825400-40827800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr21:40825400-40828000	Enhancers	K562	blood
12	chr21:40825400-40828600	Enhancers	Brain Hippocampus Middle	brain
13	chr21:40825400-40828800	Enhancers	Brain Anterior Caudate	brain
14	chr21:40825400-40829600	Weak transcription	Aorta	Aorta
15	chr21:40825600-40826400	Weak transcription	Fetal Muscle Trunk	muscle
16	chr21:40825600-40826400	Weak transcription	Right Atrium	heart
17	chr21:40825600-40828200	Enhancers	Fetal Muscle Leg	muscle
18	chr21:40825600-40836800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr21:40825800-40826600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr21:40825800-40828600	Enhancers	Brain Substantia Nigra	brain
21	chr21:40825800-40828800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr21:40826000-40826400	Weak transcription	Brain Angular Gyrus	brain
23	chr21:40826000-40827400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr21:40826000-40828000	Flanking Active TSS	Fetal Heart	heart
25	chr21:40826200-40826600	Enhancers	HSMMtube	muscle
26	chr21:40826200-40827000	Enhancers	Fetal Brain Male	brain
27	chr21:40826200-40828800	Enhancers	Skeletal Muscle Female	skeletal muscle

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