Variant report

Variant	rs7810103
Chromosome Location	chr7:147064313-147064314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:147063148..147065759-chr7:147077085..147079029,2	K562	blood:

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10500175	1.00[CHB][hapmap]
rs10500179	0.92[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10500185	1.00[CHB][hapmap]
rs10500187	1.00[CHB][hapmap]
rs11764538	1.00[CHB][hapmap]
rs11769736	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11771144	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs11772135	1.00[CHB][hapmap]
rs11773547	1.00[CHB][hapmap]
rs11773683	1.00[CHB][hapmap]
rs12703911	1.00[CHB][hapmap]
rs12703916	1.00[CHB][hapmap]
rs12703921	1.00[CHB][hapmap]
rs12703922	1.00[CHB][hapmap]
rs13221003	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs13221396	0.83[CEU][hapmap]
rs13221977	1.00[CHB][hapmap]
rs13222223	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13224292	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs13224673	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13227072	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs13227291	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs13229651	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13231364	1.00[CHB][hapmap]
rs13231991	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs13233234	0.81[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs13234094	1.00[CHB][hapmap]
rs13234757	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13235407	1.00[CHB][hapmap]
rs13235593	1.00[CHB][hapmap]
rs13236876	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs13238470	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13242678	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs13246604	1.00[CHB][hapmap]
rs13246788	1.00[CHB][hapmap]
rs13247132	1.00[CHB][hapmap]
rs13247289	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13247402	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1357896	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1404711	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1406288	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs1525227	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17223460	1.00[CHB][hapmap]
rs17224658	1.00[CHB][hapmap]
rs17412444	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs17413110	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs17497254	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs17497557	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs17498276	1.00[CHB][hapmap]
rs1842273	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs1842274	1.00[CHB][hapmap]
rs1871492	1.00[CHB][hapmap]
rs2046052	1.00[CHB][hapmap]
rs2204412	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2373031	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs2373128	1.00[CHB][hapmap]
rs2373129	1.00[CHB][hapmap]
rs34459574	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35594861	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35609387	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5028055	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs67361115	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6951143	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs6979164	1.00[CHB][hapmap]
rs73473166	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs735261	1.00[JPT][hapmap]
rs747138	1.00[CHB][hapmap]
rs7779279	0.95[CEU][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs7781303	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7781464	1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs7785125	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7798078	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs7798162	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs957484	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs997223	1.00[CHB][hapmap];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1033398	chr7:146989035-147101573	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
5	nsv465192	chr7:147001077-147086045	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
6	nsv608943	chr7:147001077-147086045	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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