Variant report

Variant	rs1881294
Chromosome Location	chr7:78959486-78959487
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10244234	0.82[AMR][1000 genomes]
rs10274885	0.89[ASN][1000 genomes]
rs10280554	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10452985	0.86[AMR][1000 genomes]
rs10485955	0.86[AMR][1000 genomes]
rs10808182	0.89[ASN][1000 genomes]
rs10953834	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11773085	0.89[ASN][1000 genomes]
rs12706097	0.87[ASN][1000 genomes]
rs1358472	0.80[ASN][1000 genomes]
rs1406165	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1406166	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1528259	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1528260	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1528264	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1528268	0.89[ASN][1000 genomes]
rs1528276	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1528278	0.83[AMR][1000 genomes]
rs1528282	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1609281	0.89[ASN][1000 genomes]
rs16886524	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16886545	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16886548	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17152178	0.91[ASN][1000 genomes]
rs17152192	0.94[ASN][1000 genomes]
rs17152223	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17152382	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1881293	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1881298	0.90[ASN][1000 genomes]
rs1918935	0.86[AMR][1000 genomes]
rs2190174	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34599162	0.86[AMR][1000 genomes]
rs41364851	0.86[AMR][1000 genomes]
rs4562253	0.81[AMR][1000 genomes]
rs55637636	0.86[AMR][1000 genomes]
rs66499867	0.86[AMR][1000 genomes]
rs66775453	0.86[AMR][1000 genomes]
rs66778115	0.86[AMR][1000 genomes]
rs66900251	0.83[AMR][1000 genomes]
rs67092648	0.83[AMR][1000 genomes]
rs67122557	0.83[AMR][1000 genomes]
rs67289031	0.86[AMR][1000 genomes]
rs67486505	0.83[AMR][1000 genomes]
rs68113978	0.84[AMR][1000 genomes]
rs6944731	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6947186	0.84[AMR][1000 genomes]
rs6954793	0.89[ASN][1000 genomes]
rs6964030	0.86[AMR][1000 genomes]
rs6964349	0.86[AMR][1000 genomes]
rs6966599	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6966753	0.86[AMR][1000 genomes]
rs6974095	0.89[ASN][1000 genomes]
rs73141612	0.83[AMR][1000 genomes]
rs73153203	0.94[ASN][1000 genomes]
rs73154930	0.94[ASN][1000 genomes]
rs73154978	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73156041	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73156043	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73156068	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73156084	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73157803	0.90[AMR][1000 genomes]
rs73157805	0.90[AMR][1000 genomes]
rs73157824	0.86[AMR][1000 genomes]
rs73157844	0.86[AMR][1000 genomes]
rs73157878	0.86[AMR][1000 genomes]
rs7455557	0.86[AMR][1000 genomes]
rs7778707	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7806210	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7811833	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9918566	0.82[AMR][1000 genomes]

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	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv831041	chr7:78819499-78973222	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2764028	chr7:78874740-79112630	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv517349	chr7:78958066-78963773	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv2762681	chr7:78958864-78982993	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:78959200-78963400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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