Variant report

Variant	rs11004557
Chromosome Location	chr10:56525095-56525096
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:56524841..56527754-chr10:56535899..56538801,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10740592	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap]
rs10763124	0.91[CHB][hapmap]
rs10763127	0.86[CHB][hapmap];0.93[CHD][hapmap]
rs10763132	0.93[ASW][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.89[MKK][hapmap];0.94[YRI][hapmap]
rs10763141	0.84[MEX][hapmap]
rs10825373	0.87[CHB][hapmap];0.86[CHD][hapmap]
rs10825387	0.93[ASW][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.89[MKK][hapmap];0.94[YRI][hapmap]
rs11004534	0.91[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs11004565	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11004568	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11004569	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11004581	0.81[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap]
rs1336193	0.88[JPT][hapmap]
rs1336201	0.87[CHB][hapmap]
rs1414691	0.87[CEU][hapmap];0.85[JPT][hapmap]
rs1591533	0.87[CHB][hapmap]
rs16906522	0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1832186	0.87[CHB][hapmap]
rs1855904	0.87[CHB][hapmap];0.83[CHD][hapmap]
rs1912985	0.87[CEU][hapmap];0.86[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1932599	0.87[CHB][hapmap]
rs1932603	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs1954616	0.80[CHB][hapmap]
rs2050545	0.93[ASW][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.89[MKK][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2050546	0.83[CHB][hapmap]
rs2050547	0.82[CHB][hapmap]
rs2065842	0.93[CEU][hapmap];0.91[CHB][hapmap];0.97[GIH][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2384523	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs4570495	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4935538	0.87[CHB][hapmap]
rs55928152	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7068489	0.87[CHB][hapmap];0.88[CHD][hapmap]
rs7091341	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7909226	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7916693	0.91[CHB][hapmap];0.85[JPT][hapmap];0.94[YRI][hapmap]
rs7918419	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050405	chr10:56224676-56800009	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv540635	chr10:56224676-56800009	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv933410	chr10:56319433-56713977	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1043144	chr10:56332903-56680265	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv550970	chr10:56361499-56764751	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	esv2758221	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2759754	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv895447	chr10:56428277-56587755	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv895448	chr10:56456576-56526747	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv526545	chr10:56462471-56554972	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1053651	chr10:56478151-56545395	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv895449	chr10:56503477-56606168	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv895450	chr10:56504373-56587755	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv895451	chr10:56504373-56606168	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv895452	chr10:56508400-56700597	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv895453	chr10:56512887-56569551	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	nsv1047184	chr10:56516350-56996193	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	nsv948015	chr10:56521935-56528691	Enhancers Weak transcription	Chromatin interactive region	n/a	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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