Variant report

Variant	rs6730174
Chromosome Location	chr2:177549478-177549479
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10497448	0.86[EUR][1000 genomes]
rs12991707	0.86[EUR][1000 genomes]
rs12997926	0.83[EUR][1000 genomes]
rs17345806	0.86[EUR][1000 genomes]
rs35231950	0.86[EUR][1000 genomes]
rs55898660	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55963234	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs66809138	0.86[EUR][1000 genomes]
rs6707447	0.82[AFR][1000 genomes]
rs72930241	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72930256	0.92[EUR][1000 genomes]
rs72930260	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72932119	0.81[AMR][1000 genomes]
rs72932120	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72932122	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72932127	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72932129	0.87[AMR][1000 genomes];0.96[EUR][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	nsv527737	chr2:177538266-177692572	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv583686	chr2:177538266-177692572	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1006500	chr2:177548521-177707097	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:177544000-177552400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:177547600-177550000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr2:177548000-177550600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:177548000-177550800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:177548000-177550800	Weak transcription	Fetal Lung	lung
6	chr2:177548600-177550000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:177548800-177550600	Weak transcription	Fetal Heart	heart

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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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