Variant report

Variant	rs10229765
Chromosome Location	chr7:126373998-126373999
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126368803..126371577-chr7:126373352..126375062,2	K562	blood:

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs1008260	1.00[JPT][hapmap]
rs10215498	0.86[JPT][hapmap]
rs10215590	0.86[JPT][hapmap]
rs10227255	0.85[JPT][hapmap]
rs10239010	0.82[JPT][hapmap]
rs10241618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10252649	0.86[JPT][hapmap]
rs10254445	1.00[JPT][hapmap]
rs10254692	0.86[JPT][hapmap]
rs10257388	0.85[JPT][hapmap]
rs10259217	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap]
rs10259229	1.00[CEU][hapmap];0.86[JPT][hapmap];0.91[YRI][hapmap]
rs10269099	1.00[CEU][hapmap]
rs10271146	0.86[JPT][hapmap]
rs10487457	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap]
rs10487459	1.00[CEU][hapmap];0.85[JPT][hapmap];0.91[YRI][hapmap]
rs10487460	0.86[JPT][hapmap]
rs10954133	0.86[JPT][hapmap]
rs11763603	0.85[JPT][hapmap]
rs11763734	0.85[JPT][hapmap]
rs11768413	1.00[JPT][hapmap]
rs11769307	0.84[CEU][hapmap];0.85[JPT][hapmap]
rs11769459	1.00[JPT][hapmap]
rs11769491	1.00[JPT][hapmap]
rs11770578	0.85[JPT][hapmap]
rs11773772	0.86[JPT][hapmap]
rs12333442	0.86[JPT][hapmap]
rs12333645	0.86[JPT][hapmap]
rs12706742	0.85[JPT][hapmap]
rs12706745	1.00[CEU][hapmap];0.85[JPT][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12706746	0.82[JPT][hapmap]
rs12706747	1.00[JPT][hapmap]
rs13222700	0.86[JPT][hapmap]
rs13224779	0.86[JPT][hapmap]
rs13225829	1.00[JPT][hapmap]
rs13226065	1.00[JPT][hapmap]
rs13226841	0.86[JPT][hapmap]
rs13236505	0.86[JPT][hapmap]
rs13240076	1.00[JPT][hapmap]
rs13240418	1.00[JPT][hapmap]
rs13242233	1.00[JPT][hapmap]
rs1361988	1.00[JPT][hapmap]
rs1361995	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs1361998	1.00[JPT][hapmap]
rs1362000	0.85[JPT][hapmap]
rs1362005	1.00[JPT][hapmap]
rs1419492	1.00[JPT][hapmap]
rs1419508	0.85[JPT][hapmap]
rs1557646	1.00[JPT][hapmap]
rs1592370	1.00[JPT][hapmap]
rs17150172	0.92[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap]
rs17619947	0.86[JPT][hapmap]
rs17620189	0.86[JPT][hapmap]
rs17620525	1.00[JPT][hapmap]
rs17626816	1.00[JPT][hapmap]
rs17627206	1.00[JPT][hapmap]
rs17683174	1.00[JPT][hapmap]
rs17683391	1.00[JPT][hapmap]
rs17693362	1.00[JPT][hapmap]
rs1946109	1.00[JPT][hapmap]
rs1946114	0.86[JPT][hapmap]
rs1946115	0.86[JPT][hapmap]
rs1989849	1.00[JPT][hapmap]
rs1989850	1.00[JPT][hapmap]
rs2023733	1.00[JPT][hapmap]
rs2023734	1.00[JPT][hapmap]
rs2023735	1.00[JPT][hapmap]
rs2106352	0.85[JPT][hapmap]
rs2106601	0.86[JPT][hapmap]
rs2157753	0.84[JPT][hapmap]
rs2157977	0.85[JPT][hapmap]
rs2157978	0.82[JPT][hapmap]
rs2157979	0.86[JPT][hapmap]
rs2214159	0.86[JPT][hapmap]
rs2283071	1.00[JPT][hapmap]
rs2283076	0.82[JPT][hapmap]
rs2283079	1.00[JPT][hapmap]
rs2299501	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs2299502	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs2299503	1.00[CEU][hapmap];0.85[JPT][hapmap]
rs2299505	1.00[CEU][hapmap];0.85[JPT][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2299506	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2299507	1.00[CEU][hapmap];0.85[JPT][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2299508	0.86[JPT][hapmap]
rs2299509	0.86[JPT][hapmap]
rs2299510	0.86[JPT][hapmap]
rs2299511	0.86[JPT][hapmap]
rs2299516	1.00[JPT][hapmap]
rs2299517	1.00[JPT][hapmap]
rs2299518	1.00[JPT][hapmap]
rs2299519	1.00[JPT][hapmap]
rs2896376	0.86[JPT][hapmap]
rs3808154	0.82[JPT][hapmap]
rs4728053	1.00[JPT][hapmap]
rs4731323	1.00[JPT][hapmap]
rs4731330	1.00[JPT][hapmap]
rs4731331	1.00[JPT][hapmap]
rs6467099	1.00[JPT][hapmap]
rs6951643	1.00[JPT][hapmap]
rs6951771	1.00[JPT][hapmap]
rs6969572	0.86[JPT][hapmap]
rs6975541	0.82[JPT][hapmap]
rs886179	0.86[JPT][hapmap]
rs929175	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs929211	1.00[JPT][hapmap]
rs950789	0.84[CEU][hapmap];0.85[JPT][hapmap]
rs954661	1.00[JPT][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: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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