Variant report

Variant	rs342692
Chromosome Location	chr13:92358166-92358167
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:92008545..92011315-chr13:92356564..92359344,2	K562	blood:
2	chr13:92357827..92359421-chr13:92380586..92382963,2	K562	blood:
3	chr13:91998255..92000962-chr13:92357552..92359516,2	K562	blood:
4	chr13:92351988..92354291-chr13:92355999..92358274,2	K562	blood:

Variant related genes	Relation type
ENSG00000215417	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10492611	0.83[EUR][1000 genomes]
rs11619422	0.83[EUR][1000 genomes]
rs11841822	0.83[EUR][1000 genomes]
rs11843202	0.83[EUR][1000 genomes]
rs11843298	0.83[EUR][1000 genomes]
rs1326742	0.84[EUR][1000 genomes]
rs1365874	0.83[EUR][1000 genomes]
rs1365875	0.83[EUR][1000 genomes]
rs1409600	0.81[EUR][1000 genomes]
rs1409602	0.83[EUR][1000 genomes]
rs1409603	0.83[EUR][1000 genomes]
rs1412311	0.84[EUR][1000 genomes]
rs1412312	0.84[EUR][1000 genomes]
rs1584154	0.83[EUR][1000 genomes]
rs163929	0.89[EUR][1000 genomes]
rs163930	0.87[EUR][1000 genomes]
rs163933	0.84[EUR][1000 genomes]
rs168216	0.87[EUR][1000 genomes]
rs16946409	0.81[EUR][1000 genomes]
rs16946412	0.81[EUR][1000 genomes]
rs16946426	0.83[EUR][1000 genomes]
rs16946459	0.83[EUR][1000 genomes]
rs1822915	0.83[EUR][1000 genomes]
rs1822916	0.83[EUR][1000 genomes]
rs182924	0.88[EUR][1000 genomes]
rs182925	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1831567	0.84[EUR][1000 genomes]
rs1831568	0.84[EUR][1000 genomes]
rs184661	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs191479	0.89[EUR][1000 genomes]
rs191480	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2882822	0.84[EUR][1000 genomes]
rs342671	0.86[EUR][1000 genomes]
rs342674	0.85[EUR][1000 genomes]
rs342675	0.86[EUR][1000 genomes]
rs342676	0.87[EUR][1000 genomes]
rs342679	0.88[EUR][1000 genomes]
rs342683	0.84[EUR][1000 genomes]
rs342684	0.89[EUR][1000 genomes]
rs342685	0.88[EUR][1000 genomes]
rs342686	0.88[EUR][1000 genomes]
rs345435	0.86[EUR][1000 genomes]
rs3852116	0.84[EUR][1000 genomes]
rs3864178	0.84[EUR][1000 genomes]
rs3906488	0.81[EUR][1000 genomes]
rs429039	0.85[EUR][1000 genomes]
rs435417	0.85[EUR][1000 genomes]
rs457538	0.85[EUR][1000 genomes]
rs460929	0.82[EUR][1000 genomes]
rs461810	0.86[EUR][1000 genomes]
rs466165	0.85[EUR][1000 genomes]
rs523428	0.86[EUR][1000 genomes]
rs532989	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs536822	0.85[EUR][1000 genomes]
rs554857	0.86[EUR][1000 genomes]
rs55924226	0.84[EUR][1000 genomes]
rs560759	0.87[EUR][1000 genomes]
rs60635585	0.83[EUR][1000 genomes]
rs6492560	0.84[EUR][1000 genomes]
rs72643220	0.81[EUR][1000 genomes]
rs72643226	0.83[EUR][1000 genomes]
rs72643228	0.83[EUR][1000 genomes]
rs7321165	0.81[EUR][1000 genomes]
rs7337822	0.85[EUR][1000 genomes]
rs914557	0.85[EUR][1000 genomes]
rs9583952	0.83[EUR][1000 genomes]
rs9589322	0.82[EUR][1000 genomes]
rs9589323	0.81[EUR][1000 genomes]
rs9589324	0.82[EUR][1000 genomes]
rs9589326	0.81[EUR][1000 genomes]
rs9589327	0.83[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	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
2	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv1049382	chr13:92024240-92521180	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv541873	chr13:92024240-92521180	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2753383	chr13:92226599-92462699	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv529268	chr13:92267310-92531263	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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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