Variant report

Variant	rs4696300
Chromosome Location	chr4:152785952-152785953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11099832	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11099833	0.82[AMR][1000 genomes]
rs11723898	0.81[AMR][1000 genomes]
rs11724664	0.82[AMR][1000 genomes]
rs12640963	0.82[CEU][hapmap]
rs13109860	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13145151	0.89[EUR][1000 genomes]
rs1872513	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1984854	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2007237	0.82[CEU][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes]
rs2062329	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3885815	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4696119	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs4696301	0.87[CEU][hapmap];0.84[GIH][hapmap];0.87[JPT][hapmap];0.83[MEX][hapmap];0.81[AMR][1000 genomes]
rs4696302	0.87[CEU][hapmap];0.84[GIH][hapmap];0.87[JPT][hapmap];0.83[MEX][hapmap];0.82[AMR][1000 genomes]
rs4696304	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv2753949	chr4:152764038-152794700	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2757086	chr4:152776271-152809738	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2759289	chr4:152776271-152809738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv16590	chr4:152778545-152790136	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1030973	chr4:152779838-152792879	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152779000-152788600	Weak transcription	Pancreas	Pancrea
2	chr4:152779200-152786000	Weak transcription	Right Ventricle	heart
3	chr4:152780800-152789000	Enhancers	Fetal Brain Male	brain
4	chr4:152781200-152794800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:152785000-152786000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:152785200-152789400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:152785400-152786400	Weak transcription	Fetal Brain Female	brain
8	chr4:152785800-152786000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
9	chr4:152785800-152786400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:152785800-152788600	Enhancers	Fetal Thymus	thymus

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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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