Variant report

Variant	rs1320552
Chromosome Location	chr6:120968061-120968062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10872209	0.87[AFR][1000 genomes]
rs12208169	0.87[AFR][1000 genomes]
rs1320554	0.87[AFR][1000 genomes]
rs1933856	0.87[AFR][1000 genomes]
rs1933857	0.87[AFR][1000 genomes]
rs1933862	0.86[AFR][1000 genomes]
rs1933863	0.86[AFR][1000 genomes]
rs1933864	0.86[AFR][1000 genomes]
rs1933865	0.87[AFR][1000 genomes]
rs1933867	0.87[AFR][1000 genomes]
rs2095813	0.86[AFR][1000 genomes]
rs2095814	0.86[AFR][1000 genomes]
rs2105185	0.86[AFR][1000 genomes]
rs2358051	0.83[AFR][1000 genomes]
rs2358052	0.87[AFR][1000 genomes]
rs2358055	0.86[AFR][1000 genomes]
rs4245507	0.87[AFR][1000 genomes]
rs4256464	0.87[AFR][1000 genomes]
rs4275089	0.87[AFR][1000 genomes]
rs4330561	0.87[AFR][1000 genomes]
rs4394257	0.87[AFR][1000 genomes]
rs4516979	0.85[AFR][1000 genomes]
rs4548042	0.87[AFR][1000 genomes]
rs4624902	0.86[AFR][1000 genomes]
rs4645454	0.85[AFR][1000 genomes]
rs4946505	0.87[AFR][1000 genomes]
rs5017483	0.87[AFR][1000 genomes]
rs6901991	0.88[AFR][1000 genomes]
rs6902004	0.87[AFR][1000 genomes]
rs6902170	0.87[AFR][1000 genomes]
rs6910126	0.87[AFR][1000 genomes]
rs6910247	0.87[AFR][1000 genomes]
rs6910364	0.85[AFR][1000 genomes]
rs6920772	0.87[AFR][1000 genomes]
rs6922392	0.87[AFR][1000 genomes]
rs6922409	0.87[AFR][1000 genomes]
rs9374959	0.86[AFR][1000 genomes]
rs9374960	0.86[AFR][1000 genomes]
rs9387874	0.86[AFR][1000 genomes]
rs9387875	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753290	chr6:120309301-120979301	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	esv2752474	chr6:120309301-120982301	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	esv2757191	chr6:120967277-121029949	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2759466	chr6:120967277-121029949	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv886586	chr6:120968061-121020821	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:120966600-120968600	Enhancers	Fetal Lung	lung
2	chr6:120967800-120968200	Enhancers	Fetal Brain Male	brain

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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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