Variant report

Variant	rs17385455
Chromosome Location	chr7:78351701-78351702
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1012955	1.00[CHB][hapmap]
rs10244070	1.00[CHB][hapmap]
rs10485911	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10953690	1.00[CHB][hapmap]
rs1207863	1.00[CHB][hapmap]
rs1207864	1.00[CHB][hapmap]
rs1207865	1.00[CHB][hapmap]
rs1207867	1.00[CHB][hapmap]
rs1207894	1.00[CHB][hapmap]
rs12705771	1.00[CHB][hapmap]
rs1496767	1.00[CHB][hapmap]
rs1496772	1.00[ASN][1000 genomes]
rs16886302	1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs17151352	0.91[CEU][hapmap];0.81[AMR][1000 genomes]
rs17151376	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs17151525	1.00[CHB][hapmap]
rs17151530	1.00[CHB][hapmap]
rs17383882	1.00[ASN][1000 genomes]
rs17450323	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17450926	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1989977	1.00[CHB][hapmap]
rs1989978	1.00[CHB][hapmap]
rs246463	1.00[CHB][hapmap]
rs2525808	1.00[CHB][hapmap]
rs2774059	1.00[CHB][hapmap]
rs37847	1.00[CHB][hapmap]
rs37848	1.00[CHB][hapmap]
rs37850	1.00[CHB][hapmap]
rs37862	1.00[CHB][hapmap]
rs37863	1.00[CHB][hapmap]
rs37871	1.00[CHB][hapmap]
rs37872	1.00[CHB][hapmap]
rs37873	1.00[CHB][hapmap]
rs37884	1.00[CHB][hapmap]
rs39731	1.00[CHB][hapmap]
rs55934210	0.84[AFR][1000 genomes]
rs56364307	1.00[ASN][1000 genomes]
rs60460465	0.81[AFR][1000 genomes]
rs73380292	1.00[ASN][1000 genomes]
rs73702968	1.00[ASN][1000 genomes]
rs7780363	1.00[CHB][hapmap]
rs886472	1.00[CHB][hapmap]
rs886473	1.00[CHB][hapmap]
rs886474	1.00[CHB][hapmap]
rs970757	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1019355	chr7:78319575-78399845	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78346800-78352800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:78346800-78361400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr7:78349000-78352200	Enhancers	Fetal Heart	heart
4	chr7:78351600-78351800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr7:78351600-78351800	Enhancers	Skeletal Muscle Female	skeletal muscle

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