Variant report

Variant	rs34518941
Chromosome Location	chr2:167620924-167620925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10427382	0.82[AMR][1000 genomes]
rs1605877	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs16852633	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2390429	0.81[AFR][1000 genomes]
rs2655827	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2655837	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4274612	0.81[AFR][1000 genomes]
rs59533882	0.82[AMR][1000 genomes]
rs73020308	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs73020311	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs73020312	0.94[AMR][1000 genomes]
rs73970082	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7590350	0.81[AFR][1000 genomes]
rs964215	0.86[AFR][1000 genomes];0.81[AMR][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	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875375	chr2:167515013-167703912	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:167620200-167623600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:167620400-167621000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr2:167620400-167623200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:167620600-167621000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr2:167620800-167621000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:167620800-167621200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:167620800-167623000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:167620800-167623200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:167620800-167623200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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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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