Variant report

Variant	rs17009037
Chromosome Location	chr1:221083285-221083286
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:18)

rs_ID	r²[population]
rs10495153	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10495154	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11806418	0.93[EUR][1000 genomes]
rs11809417	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12565509	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12566858	0.93[EUR][1000 genomes]
rs12567705	0.90[EUR][1000 genomes]
rs12568739	0.93[EUR][1000 genomes]
rs17009060	0.90[EUR][1000 genomes]
rs17009078	0.93[EUR][1000 genomes]
rs2807861	0.81[ASN][1000 genomes]
rs35014198	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3820355	0.87[ASN][1000 genomes]
rs6541166	0.94[ASN][1000 genomes]
rs6678259	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73108353	0.94[ASN][1000 genomes]
rs7418458	0.93[EUR][1000 genomes]
rs945447	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 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	chr1:221080600-221090200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:221082200-221087200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:221082400-221087000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:221082400-221087200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr1:221082400-221087400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr1:221082600-221086800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:221082600-221087600	Weak transcription	Liver	Liver

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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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