Variant report

Variant	rs59787482
Chromosome Location	chr6:77777381-77777382
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 115 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1022756	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10428816	0.86[EUR][1000 genomes]
rs1072272	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10806080	0.87[EUR][1000 genomes]
rs10806081	0.87[EUR][1000 genomes]
rs10943402	0.87[EUR][1000 genomes]
rs10943407	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10943408	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10943409	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10943414	0.84[ASN][1000 genomes]
rs10943417	0.80[ASN][1000 genomes]
rs11756500	0.87[EUR][1000 genomes]
rs12526385	0.87[EUR][1000 genomes]
rs12527772	0.87[EUR][1000 genomes]
rs12527884	0.82[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs12530165	0.87[EUR][1000 genomes]
rs1322085	0.87[EUR][1000 genomes]
rs1322086	0.86[EUR][1000 genomes]
rs1322087	0.87[EUR][1000 genomes]
rs1322088	0.87[EUR][1000 genomes]
rs1322089	0.87[EUR][1000 genomes]
rs1322090	0.87[EUR][1000 genomes]
rs1548241	0.84[ASN][1000 genomes]
rs1575242	0.87[EUR][1000 genomes]
rs16888396	0.87[EUR][1000 genomes]
rs16888412	0.87[EUR][1000 genomes]
rs16888440	0.87[EUR][1000 genomes]
rs1923341	0.87[EUR][1000 genomes]
rs2320210	0.84[ASN][1000 genomes]
rs34832629	0.87[EUR][1000 genomes]
rs4365896	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4706641	0.87[EUR][1000 genomes]
rs4708309	0.87[EUR][1000 genomes]
rs4708310	0.87[EUR][1000 genomes]
rs4708311	0.87[EUR][1000 genomes]
rs4708314	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55652257	0.87[EUR][1000 genomes]
rs55794868	0.87[EUR][1000 genomes]
rs55840940	0.87[EUR][1000 genomes]
rs55927662	0.87[EUR][1000 genomes]
rs56043984	0.87[EUR][1000 genomes]
rs57144450	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57433966	0.87[EUR][1000 genomes]
rs57437071	0.87[EUR][1000 genomes]
rs58791359	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59010538	0.87[EUR][1000 genomes]
rs59696630	0.87[EUR][1000 genomes]
rs62433587	0.87[EUR][1000 genomes]
rs66460821	0.87[EUR][1000 genomes]
rs6912149	0.99[ASN][1000 genomes]
rs6912561	1.00[ASN][1000 genomes]
rs6912606	1.00[ASN][1000 genomes]
rs6912721	1.00[ASN][1000 genomes]
rs6913599	0.84[ASN][1000 genomes]
rs6916958	0.95[ASN][1000 genomes]
rs6923177	0.87[EUR][1000 genomes]
rs6923352	0.87[EUR][1000 genomes]
rs6929259	0.99[ASN][1000 genomes]
rs6937055	0.91[EUR][1000 genomes]
rs7450963	0.87[EUR][1000 genomes]
rs7453658	0.87[EUR][1000 genomes]
rs7738950	0.87[EUR][1000 genomes]
rs7738957	0.85[EUR][1000 genomes]
rs7739351	0.87[EUR][1000 genomes]
rs7740676	0.87[EUR][1000 genomes]
rs7740860	0.87[EUR][1000 genomes]
rs7752644	0.87[EUR][1000 genomes]
rs7772213	0.87[EUR][1000 genomes]
rs7772246	0.87[EUR][1000 genomes]
rs7773420	0.85[EUR][1000 genomes]
rs7773651	0.87[EUR][1000 genomes]
rs7776431	0.84[ASN][1000 genomes]
rs926650	0.90[EUR][1000 genomes]
rs926651	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs926652	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs9294054	0.83[EUR][1000 genomes]
rs9294055	0.87[EUR][1000 genomes]
rs9341627	0.87[EUR][1000 genomes]
rs9341631	0.87[EUR][1000 genomes]
rs9343540	0.87[EUR][1000 genomes]
rs9343541	0.87[EUR][1000 genomes]
rs9343542	0.87[EUR][1000 genomes]
rs9343543	0.87[EUR][1000 genomes]
rs9343545	0.87[EUR][1000 genomes]
rs9343560	0.80[ASN][1000 genomes]
rs9343562	0.80[ASN][1000 genomes]
rs9350690	0.87[EUR][1000 genomes]
rs9352425	0.87[EUR][1000 genomes]
rs9352426	0.87[EUR][1000 genomes]
rs9352427	0.87[EUR][1000 genomes]
rs9352433	0.99[ASN][1000 genomes]
rs9359236	0.87[EUR][1000 genomes]
rs9359238	0.87[EUR][1000 genomes]
rs9359247	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9361179	0.87[EUR][1000 genomes]
rs9361180	0.87[EUR][1000 genomes]
rs9361185	0.90[EUR][1000 genomes]
rs9361191	0.84[ASN][1000 genomes]
rs978310	0.84[ASN][1000 genomes]
rs9800888	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019520	chr6:77355212-77875164	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv538321	chr6:77355212-77875164	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv603806	chr6:77587889-77787815	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1021812	chr6:77589219-77792085	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1030186	chr6:77606604-77781304	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1026517	chr6:77622310-77827418	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv3417770	chr6:77670473-77963253	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv3402238	chr6:77670497-77963278	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1022311	chr6:77684420-77941524	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv886223	chr6:77686247-77950949	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv603807	chr6:77734250-77807794	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv1033731	chr6:77750293-77941524	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv538323	chr6:77750293-77941524	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77773800-77779000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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