Variant report

Variant	rs12629256
Chromosome Location	chr3:150552178-150552179
allele	A/T
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]
rs10513379	0.92[EUR][1000 genomes]
rs1444198	0.92[CEU][hapmap];0.81[YRI][hapmap];0.88[EUR][1000 genomes]
rs1444199	0.88[EUR][1000 genomes]
rs16862877	0.92[CEU][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16862928	0.84[EUR][1000 genomes]
rs2034158	0.88[EUR][1000 genomes]
rs2037408	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs2037409	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs56659353	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58515064	0.87[EUR][1000 genomes]
rs60107900	0.87[EUR][1000 genomes]
rs60336215	0.90[EUR][1000 genomes]
rs60979559	0.91[EUR][1000 genomes]
rs61132047	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67193230	0.84[EUR][1000 genomes]
rs73152585	0.88[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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv818177	chr3:150541363-150566422	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150550600-150556200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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