Variant report

Variant	rs7703511
Chromosome Location	chr5:88841718-88841719
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16867725	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16867731	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16867735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16867737	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6864255	1.00[ASN][1000 genomes]
rs6864306	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6875048	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6875289	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6875893	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6878379	1.00[EUR][1000 genomes]
rs73770511	0.96[ASN][1000 genomes]
rs73772196	1.00[ASN][1000 genomes]
rs73772197	1.00[ASN][1000 genomes]
rs7709961	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7722957	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533373	chr5:88062497-89028098	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
2	nsv830389	chr5:88669984-88860383	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1845994	chr5:88736275-88847756	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:88840600-88842400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:88840600-88843000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:88841000-88842200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr5:88841000-88842600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:88841200-88842800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:88841200-88842800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr5:88841200-88843000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:88841400-88842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:88841400-88842200	Enhancers	Colon Smooth Muscle	Colon
10	chr5:88841400-88842200	Enhancers	Fetal Brain Male	brain
11	chr5:88841400-88842200	Enhancers	Fetal Brain Female	brain
12	chr5:88841400-88842800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:88841600-88842800	Enhancers	HUES6 Cell Line	embryonic stem cell

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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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