Variant report

Variant	rs10768352
Chromosome Location	chr11:4918795-4918796
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4918642..4921294-chr11:5101983..5104188,2	K562	blood:
2	chr11:4912456..4914892-chr11:4916437..4919051,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10836748	1.00[CHB][hapmap]
rs10836850	1.00[CHB][hapmap]
rs10836868	1.00[CHB][hapmap]
rs10836896	1.00[CHB][hapmap]
rs10836912	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10836949	1.00[YRI][hapmap]
rs10836950	1.00[YRI][hapmap]
rs10836954	1.00[YRI][hapmap]
rs10836955	1.00[YRI][hapmap]
rs10836956	1.00[YRI][hapmap]
rs11034193	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11034203	1.00[CHB][hapmap]
rs11034360	1.00[CHB][hapmap]
rs11034368	1.00[CHB][hapmap]
rs11034418	1.00[CHB][hapmap]
rs11034428	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs11034429	1.00[CHB][hapmap]
rs11034467	1.00[CHB][hapmap]
rs11034493	1.00[CHB][hapmap]
rs11034541	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs11034563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11034615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11034672	1.00[YRI][hapmap]
rs11600256	1.00[CHB][hapmap]
rs11601065	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11602499	1.00[CHB][hapmap]
rs12273277	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12276692	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12291286	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12291506	1.00[JPT][hapmap]
rs12360722	1.00[CHB][hapmap]
rs12361514	1.00[CHB][hapmap]
rs12361955	1.00[CHB][hapmap]
rs12364864	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1347274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1368823	1.00[CHB][hapmap]
rs1368824	1.00[CHB][hapmap]
rs1433917	1.00[CHB][hapmap]
rs1583350	1.00[CHB][hapmap]
rs16906639	1.00[CHB][hapmap]
rs17250052	1.00[CHB][hapmap]
rs17250577	1.00[CHB][hapmap]
rs17252989	1.00[CHB][hapmap]
rs17330155	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1816448	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1865286	1.00[CHB][hapmap]
rs2570591	1.00[CHB][hapmap]
rs4910693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7116979	1.00[YRI][hapmap]
rs7949235	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048224	chr11:4390227-4920324	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
2	nsv540917	chr11:4390227-4920324	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	esv2758254	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
5	esv2759799	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
6	nsv8781	chr11:4916743-4921311	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	n/a	diseases
7	nsv896917	chr11:4917089-4935470	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island 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
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