Variant report

Variant	rs5030278
Chromosome Location	chr11:32417526-32417527
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12271917	1.00[CHB][hapmap]
rs16923250	1.00[JPT][hapmap]
rs16923260	1.00[JPT][hapmap]
rs17673047	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs2234593	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28460016	0.86[ASN][1000 genomes]
rs5030228	1.00[JPT][hapmap]
rs5030255	0.86[ASN][1000 genomes]
rs5030302	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs5030311	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes]
rs5030315	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030335	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs59961456	0.86[ASN][1000 genomes]
rs7105471	1.00[CEU][hapmap];0.86[ASN][1000 genomes]
rs7120483	1.00[ASN][1000 genomes]
rs73473736	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1038188	chr11:32410305-32449799	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32408600-32421600	Weak transcription	Left Ventricle	heart
2	chr11:32409400-32422000	Weak transcription	Fetal Kidney	kidney
3	chr11:32412000-32417800	Weak transcription	Right Ventricle	heart
4	chr11:32412200-32418000	Weak transcription	Spleen	Spleen
5	chr11:32412400-32417600	Weak transcription	Ovary	ovary
6	chr11:32412600-32421800	Strong transcription	K562	blood
7	chr11:32414400-32418200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:32414800-32424200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:32415200-32418000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:32415200-32418600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:32415400-32418000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:32416200-32418600	Enhancers	Fetal Heart	heart
13	chr11:32417200-32419000	Flanking Active TSS	Dnd41	blood

Quick Search:

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

what's new

Quick links