Variant report

Variant	rs71327064
Chromosome Location	chr3:46478866-46478867
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11574430	0.85[EUR][1000 genomes]
rs11574436	0.85[EUR][1000 genomes]
rs17141079	0.82[EUR][1000 genomes]
rs17141101	0.85[EUR][1000 genomes]
rs34200951	0.84[EUR][1000 genomes]
rs34953706	0.82[EUR][1000 genomes]
rs35878193	0.84[EUR][1000 genomes]
rs6777875	0.82[EUR][1000 genomes]
rs71327061	0.83[EUR][1000 genomes]
rs71327062	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3323840	chr3:46352348-46497196	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv3389382	chr3:46352798-46496696	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1014624	chr3:46463424-46549188	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1013306	chr3:46469014-46698538	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46455800-46496800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:46459400-46491600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr3:46465200-46488800	Weak transcription	Left Ventricle	heart
4	chr3:46465200-46488800	Weak transcription	Right Ventricle	heart
5	chr3:46474600-46480600	Strong transcription	Spleen	Spleen
6	chr3:46474800-46480400	Weak transcription	Thymus	Thymus
7	chr3:46474800-46481800	Weak transcription	Primary B cells from cord blood	blood
8	chr3:46477400-46479600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:46477400-46479600	Weak transcription	Fetal Thymus	thymus
10	chr3:46477400-46480000	Weak transcription	Lung	lung
11	chr3:46477400-46484200	Weak transcription	Fetal Intestine Small	intestine
12	chr3:46477600-46479600	Weak transcription	Primary T cells from cord blood	blood
13	chr3:46477600-46479800	Weak transcription	Dnd41	blood
14	chr3:46478200-46480600	Weak transcription	Gastric	stomach
15	chr3:46478400-46480600	Weak transcription	Adipose Nuclei	Adipose
16	chr3:46478400-46480600	Weak transcription	Pancreas	Pancrea

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Input of quick search could be:

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

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