Variant report

Variant	rs17053363
Chromosome Location	chr3:53736557-53736558
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13063116	0.82[GIH][hapmap]
rs1380608	1.00[CEU][hapmap];0.93[GIH][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17053338	1.00[GIH][hapmap]
rs34804225	0.97[EUR][1000 genomes]
rs3774487	0.93[GIH][hapmap]
rs3774490	0.93[GIH][hapmap]
rs3774503	0.93[GIH][hapmap]
rs71301850	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7651668	0.84[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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53683200-53744200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr3:53715600-53739600	Weak transcription	Brain Anterior Caudate	brain
3	chr3:53721000-53739800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:53723200-53743400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:53724800-53739400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:53726600-53744000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr3:53726800-53743400	Weak transcription	Spleen	Spleen
8	chr3:53731600-53737800	Weak transcription	Right Atrium	heart
9	chr3:53734600-53738600	Weak transcription	Fetal Muscle Leg	muscle
10	chr3:53734600-53739000	Strong transcription	Fetal Intestine Small	intestine
11	chr3:53735400-53738200	Strong transcription	Fetal Lung	lung
12	chr3:53735600-53737400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr3:53735600-53740600	Strong transcription	Fetal Intestine Large	intestine
14	chr3:53736200-53738400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr3:53736200-53738600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:53736200-53738800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:53736200-53740600	Enhancers	Fetal Thymus	thymus
18	chr3:53736400-53736600	Enhancers	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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