Variant report

Variant	rs1362000
Chromosome Location	chr7:126401715-126401716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126400783..126403060-chr7:126405651..126408997,3	K562	blood:

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs1008260	0.88[CEU][hapmap]
rs10215498	0.93[CEU][hapmap]
rs10215590	0.93[CEU][hapmap]
rs10216287	0.93[CEU][hapmap]
rs10229765	0.85[JPT][hapmap]
rs10239010	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs10250459	0.93[CEU][hapmap]
rs10252649	0.93[CEU][hapmap]
rs10254445	0.92[CEU][hapmap]
rs10254692	0.93[CEU][hapmap]
rs10271146	0.93[CEU][hapmap]
rs10487460	0.93[CEU][hapmap]
rs10954133	0.92[CEU][hapmap]
rs11763603	0.92[CEU][hapmap]
rs11763734	0.92[CEU][hapmap]
rs11765100	0.96[CEU][hapmap]
rs11768413	1.00[JPT][hapmap]
rs11769459	0.93[CEU][hapmap]
rs11769491	0.92[CEU][hapmap]
rs11770578	0.92[CEU][hapmap]
rs11773772	0.91[CEU][hapmap]
rs12333442	0.93[CEU][hapmap]
rs12333645	0.93[CEU][hapmap]
rs12706747	0.89[CEU][hapmap]
rs13222700	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs13224779	0.93[CEU][hapmap]
rs13225829	0.88[CEU][hapmap]
rs13226065	0.93[CEU][hapmap]
rs13226841	0.92[CEU][hapmap]
rs13236505	0.93[CEU][hapmap]
rs13240076	0.84[CEU][hapmap]
rs13240418	0.88[CEU][hapmap]
rs1361998	0.93[CEU][hapmap]
rs1361999	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1362002	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1362004	0.93[CEU][hapmap]
rs1419508	0.92[CEU][hapmap]
rs1557646	0.89[CEU][hapmap]
rs1592370	0.96[CEU][hapmap]
rs17619947	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs17620189	0.93[CEU][hapmap]
rs17620525	0.93[CEU][hapmap]
rs17626816	0.91[CEU][hapmap]
rs17627206	0.92[CEU][hapmap]
rs17683174	0.92[CEU][hapmap]
rs17683391	0.92[CEU][hapmap]
rs17693362	0.93[CEU][hapmap]
rs1946109	0.93[CEU][hapmap]
rs1946114	0.93[CEU][hapmap]
rs1946115	0.93[CEU][hapmap]
rs1989849	0.92[CEU][hapmap]
rs1989850	0.92[CEU][hapmap]
rs2023733	0.89[CEU][hapmap]
rs2023734	0.92[CEU][hapmap]
rs2023735	0.92[CEU][hapmap]
rs2106600	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs2106601	0.93[CEU][hapmap]
rs2157977	0.92[CEU][hapmap]
rs2157978	0.92[CEU][hapmap]
rs2157979	0.93[CEU][hapmap]
rs2214159	0.92[CEU][hapmap]
rs2283071	0.88[CEU][hapmap]
rs2299508	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs2299509	0.93[CEU][hapmap]
rs2299510	0.93[CEU][hapmap]
rs2299511	0.93[CEU][hapmap]
rs2299516	0.96[CEU][hapmap]
rs2299517	0.92[CEU][hapmap]
rs2299518	0.92[CEU][hapmap]
rs2299519	0.92[CEU][hapmap]
rs2299520	0.93[CEU][hapmap]
rs2896376	0.92[CEU][hapmap]
rs35825148	0.85[EUR][1000 genomes]
rs4728053	0.89[CEU][hapmap]
rs4731330	0.92[CEU][hapmap]
rs6467099	0.93[CEU][hapmap]
rs6951643	0.92[CEU][hapmap]
rs6951771	0.92[CEU][hapmap]
rs6969572	0.93[CEU][hapmap]
rs727903	0.93[CEU][hapmap]
rs886179	0.93[CEU][hapmap]
rs929211	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs954661	0.92[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032938	chr7:126067684-126587859	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539119	chr7:126067684-126587859	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv889187	chr7:126219766-126478190	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126401400-126401800	Enhancers	GM12878-XiMat	blood

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