Variant report

Variant	rs1540514
Chromosome Location	chr1:190301470-190301471
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1031076	0.85[JPT][hapmap];1.00[YRI][hapmap]
rs10800939	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10920661	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.83[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10920663	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10920672	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10920673	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10920674	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10920675	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10920681	0.86[CHB][hapmap];0.85[JPT][hapmap];0.85[YRI][hapmap]
rs10920684	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.92[YRI][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10920691	0.85[CEU][hapmap]
rs1148611	0.92[AFR][1000 genomes]
rs1148613	0.85[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs1171148	0.83[YRI][hapmap]
rs1171149	0.87[JPT][hapmap];0.84[YRI][hapmap]
rs1171335	0.80[JPT][hapmap];0.81[YRI][hapmap];0.85[AFR][1000 genomes]
rs1171339	0.90[AFR][1000 genomes]
rs1171374	0.86[JPT][hapmap]
rs1171384	0.94[JPT][hapmap];1.00[YRI][hapmap]
rs1180451	0.86[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs1185314	0.85[JPT][hapmap]
rs12022837	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12025655	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12117477	0.94[CEU][hapmap];0.89[CHB][hapmap];0.80[JPT][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12118393	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12122665	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12125097	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12129085	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12130069	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12135499	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap]
rs12137081	1.00[CEU][hapmap]
rs12140456	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12564065	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12742833	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1342913	0.95[CEU][hapmap];0.83[YRI][hapmap]
rs1412966	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1412970	0.95[CEU][hapmap];0.85[CHB][hapmap];0.83[JPT][hapmap];0.83[YRI][hapmap]
rs1412972	0.95[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1418803	0.95[CEU][hapmap];0.83[YRI][hapmap]
rs1592250	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1726565	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17481	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[YRI][hapmap]
rs1759762	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1759764	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1782560	0.85[JPT][hapmap];1.00[YRI][hapmap]
rs1819496	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1819497	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1831781	1.00[CEU][hapmap];0.85[CHB][hapmap];0.83[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1855239	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1880906	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2184108	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2247204	0.95[CEU][hapmap];0.85[CHB][hapmap];0.85[YRI][hapmap]
rs2247300	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs2265670	0.82[CEU][hapmap]
rs34545805	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35971648	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs36020344	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4255389	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4463673	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4611014	0.83[AMR][1000 genomes]
rs4622069	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs480692	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs504631	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs505600	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs529018	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs567393	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs591273	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs636366	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs651660	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs652953	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6697765	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs682818	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs703928	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs718608	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap]
rs725106	0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7511657	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7523618	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7542545	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs815158	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs815161	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs815336	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs815337	0.81[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs815338	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs815339	0.95[CEU][hapmap];0.81[CHB][hapmap];0.83[YRI][hapmap]
rs815348	1.00[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];0.85[YRI][hapmap]
rs860091	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs963796	0.86[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv548532	chr1:189758772-190371671	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv932040	chr1:190005334-190914580	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1013402	chr1:190197674-190332464	Enhancers ZNF genes & repeats Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	nsv535246	chr1:190197674-190332464	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	nsv1004868	chr1:190259314-190303769	Enhancers Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
6	nsv535247	chr1:190259314-190303769	Enhancers Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
7	nsv1007121	chr1:190263588-190305514	Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
8	nsv430013	chr1:190288297-190351677	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	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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