Variant report

Variant	rs13312787
Chromosome Location	chr12:4481966-4481967
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1005054	0.94[EUR][1000 genomes]
rs10735033	0.88[ASW][hapmap];1.00[GIH][hapmap];0.84[YRI][hapmap]
rs10744644	0.94[EUR][1000 genomes]
rs10774228	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs10774229	0.94[EUR][1000 genomes]
rs10849052	0.94[EUR][1000 genomes]
rs11063125	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11063126	1.00[EUR][1000 genomes]
rs11063223	1.00[CEU][hapmap]
rs2011618	1.00[EUR][1000 genomes]
rs2358726	0.85[AFR][1000 genomes]
rs2970807	0.88[EUR][1000 genomes]
rs7138225	0.82[EUR][1000 genomes]
rs7295857	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7310365	0.90[AFR][1000 genomes]
rs7313282	1.00[CEU][hapmap];1.00[EUR][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	nsv530520	chr12:3726841-4601757	Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv557123	chr12:4436632-4736569	Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4465200-4488400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:4478600-4484200	Strong transcription	Fetal Intestine Large	intestine
3	chr12:4480400-4484400	Weak transcription	Fetal Intestine Small	intestine

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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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