Variant report

Variant	rs73005814
Chromosome Location	chr3:150530065-150530066
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1373418	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1814463	0.82[EUR][1000 genomes]
rs1814464	0.82[EUR][1000 genomes]
rs2014279	0.82[EUR][1000 genomes]
rs2018246	0.82[EUR][1000 genomes]
rs34348847	0.82[EUR][1000 genomes]
rs34771595	0.82[EUR][1000 genomes]
rs3851356	0.82[EUR][1000 genomes]
rs41354246	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs57278175	0.82[EUR][1000 genomes]
rs57869178	0.82[EUR][1000 genomes]
rs60259684	0.82[EUR][1000 genomes]
rs6440696	0.82[EUR][1000 genomes]
rs6440697	0.94[EUR][1000 genomes]
rs6440698	0.94[EUR][1000 genomes]
rs6440699	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6768306	0.86[ASN][1000 genomes]
rs6769917	0.82[EUR][1000 genomes]
rs6777178	0.82[EUR][1000 genomes]
rs6792791	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6795396	0.82[EUR][1000 genomes]
rs6805481	0.82[EUR][1000 genomes]
rs6806197	0.82[EUR][1000 genomes]
rs73003787	0.82[EUR][1000 genomes]
rs73003792	0.82[EUR][1000 genomes]
rs73005813	0.81[AMR][1000 genomes]
rs73010941	0.82[EUR][1000 genomes]
rs73010947	0.82[EUR][1000 genomes]
rs73010956	0.82[EUR][1000 genomes]
rs73010964	0.82[EUR][1000 genomes]
rs73010965	0.82[EUR][1000 genomes]
rs73869297	0.82[EUR][1000 genomes]
rs7617507	0.82[EUR][1000 genomes]
rs7628481	0.82[EUR][1000 genomes]
rs7628776	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150524800-150530200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:150525200-150530200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:150529800-150530400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:150529800-150530400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:150529800-150531600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr3:150530000-150530200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:150530000-150530400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:150530000-150531000	Enhancers	Ovary	ovary

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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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