Variant report

Variant	rs1812168
Chromosome Location	chr4:152833826-152833827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10028709	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10517561	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11099832	0.92[EUR][1000 genomes]
rs11099833	0.93[EUR][1000 genomes]
rs11099834	0.95[EUR][1000 genomes]
rs11723898	0.93[EUR][1000 genomes]
rs11724664	0.96[EUR][1000 genomes]
rs11731150	0.98[EUR][1000 genomes]
rs12640963	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[YRI][hapmap];0.95[EUR][1000 genomes]
rs13124587	0.96[EUR][1000 genomes]
rs17028150	0.98[EUR][1000 genomes]
rs2007237	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4696119	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[YRI][hapmap];0.96[EUR][1000 genomes]
rs4696301	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs4696302	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs4696304	0.96[EUR][1000 genomes]
rs4696305	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4696306	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	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	nsv1030328	chr4:152791533-152875666	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1028836	chr4:152791680-152879097	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152831600-152838400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:152832800-152834000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:152833000-152834000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:152833000-152834000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:152833000-152834800	Enhancers	Thymus	Thymus
6	chr4:152833200-152834000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:152833200-152834000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:152833200-152834000	Enhancers	GM12878-XiMat	blood
9	chr4:152833200-152834200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr4:152833200-152834200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr4:152833200-152834200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:152833400-152834200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:152833600-152834400	Flanking Active TSS	Fetal Thymus	thymus
14	chr4:152833600-152838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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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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