Variant report

Variant	rs56095249
Chromosome Location	chr4:143701951-143701952
allele	A/G
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:19)

rs_ID	r²[population]
rs12331053	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17016765	1.00[EUR][1000 genomes]
rs17016793	0.94[EUR][1000 genomes]
rs28542032	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28647363	1.00[EUR][1000 genomes]
rs28753896	1.00[EUR][1000 genomes]
rs55780736	1.00[EUR][1000 genomes]
rs55785946	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55909030	1.00[AMR][1000 genomes]
rs56027664	1.00[EUR][1000 genomes]
rs56158313	1.00[EUR][1000 genomes]
rs56254574	1.00[EUR][1000 genomes]
rs56258617	1.00[EUR][1000 genomes]
rs56267841	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56293642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56377132	1.00[EUR][1000 genomes]
rs6812076	1.00[EUR][1000 genomes]
rs6814777	1.00[EUR][1000 genomes]
rs6832375	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	nsv595606	chr4:143631691-143729595	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880174	chr4:143639498-143848024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143684200-143706000	Weak transcription	Fetal Heart	heart
2	chr4:143698400-143719000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:143698800-143704600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:143698800-143738600	Weak transcription	Aorta	Aorta
5	chr4:143699000-143714600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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