Variant report

Variant	rs1637495
Chromosome Location	chr7:87604188-87604189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10235694	0.83[EUR][1000 genomes]
rs10241669	0.83[EUR][1000 genomes]
rs10266440	0.83[EUR][1000 genomes]
rs10279940	0.83[EUR][1000 genomes]
rs10282572	0.83[EUR][1000 genomes]
rs10952906	0.83[EUR][1000 genomes]
rs11770982	0.82[EUR][1000 genomes]
rs11972409	0.84[EUR][1000 genomes]
rs1201841	0.95[ASN][1000 genomes]
rs12669586	0.83[EUR][1000 genomes]
rs12704375	0.83[EUR][1000 genomes]
rs12704380	0.86[EUR][1000 genomes]
rs12704381	0.86[EUR][1000 genomes]
rs1613737	0.85[EUR][1000 genomes]
rs1623535	0.86[EUR][1000 genomes]
rs1629569	0.87[EUR][1000 genomes]
rs1631368	0.85[EUR][1000 genomes]
rs1637487	0.87[EUR][1000 genomes]
rs1637488	0.86[EUR][1000 genomes]
rs1637489	0.86[EUR][1000 genomes]
rs1637490	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1637492	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1637494	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1637496	0.87[EUR][1000 genomes]
rs1637497	0.87[EUR][1000 genomes]
rs1637498	0.87[EUR][1000 genomes]
rs1637499	0.87[EUR][1000 genomes]
rs1637500	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1637502	0.87[EUR][1000 genomes]
rs1637503	0.86[EUR][1000 genomes]
rs1637504	0.84[EUR][1000 genomes]
rs1637505	0.81[EUR][1000 genomes]
rs1637506	0.85[EUR][1000 genomes]
rs1637508	0.84[EUR][1000 genomes]
rs1637509	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1637511	0.87[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1688886	0.88[EUR][1000 genomes]
rs1688887	0.87[EUR][1000 genomes]
rs1688888	0.87[EUR][1000 genomes]
rs1688890	0.87[EUR][1000 genomes]
rs1688891	0.87[EUR][1000 genomes]
rs1688893	0.86[EUR][1000 genomes]
rs1688894	0.86[EUR][1000 genomes]
rs1688895	0.86[EUR][1000 genomes]
rs1688896	0.86[EUR][1000 genomes]
rs1688897	0.86[EUR][1000 genomes]
rs1688898	0.85[EUR][1000 genomes]
rs1688899	0.85[EUR][1000 genomes]
rs1688901	0.86[EUR][1000 genomes]
rs17150161	0.81[EUR][1000 genomes]
rs2021741	0.83[EUR][1000 genomes]
rs2022160	0.85[EUR][1000 genomes]
rs2022163	0.84[EUR][1000 genomes]
rs2022164	0.84[EUR][1000 genomes]
rs2023533	0.85[EUR][1000 genomes]
rs2079422	0.83[EUR][1000 genomes]
rs2079423	0.83[EUR][1000 genomes]
rs2097917	0.82[EUR][1000 genomes]
rs2158766	0.84[EUR][1000 genomes]
rs2282948	0.85[EUR][1000 genomes]
rs2282949	0.84[EUR][1000 genomes]
rs2373486	0.82[EUR][1000 genomes]
rs2373487	0.83[EUR][1000 genomes]
rs28794871	0.83[EUR][1000 genomes]
rs4728718	0.86[EUR][1000 genomes]
rs56160917	0.83[EUR][1000 genomes]
rs56897831	0.82[EUR][1000 genomes]
rs59135798	0.80[EUR][1000 genomes]
rs60069756	0.82[EUR][1000 genomes]
rs6465124	0.82[EUR][1000 genomes]
rs7786538	0.81[EUR][1000 genomes]
rs7803521	0.86[EUR][1000 genomes]
rs9641021	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	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv525073	chr7:87535096-87812968	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv517676	chr7:87603743-87606246	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87591200-87610800	Weak transcription	Brain Anterior Caudate	brain
2	chr7:87594400-87618000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:87600200-87605200	Weak transcription	GM12878-XiMat	blood
4	chr7:87600400-87610800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:87601000-87607400	Weak transcription	Dnd41	blood

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