Variant report

Variant	rs17649154
Chromosome Location	chr7:13680235-13680236
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10228502	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10243935	0.90[ASN][1000 genomes]
rs10244162	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10258560	0.85[ASN][1000 genomes]
rs10258748	0.85[ASN][1000 genomes]
rs10258755	0.85[ASN][1000 genomes]
rs10263971	0.86[ASN][1000 genomes]
rs10266134	0.85[ASN][1000 genomes]
rs10272801	0.85[ASN][1000 genomes]
rs10499432	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12111602	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12539609	0.96[CEU][hapmap];0.95[CHB][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13232273	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1404943	0.86[ASN][1000 genomes]
rs2056646	0.83[EUR][1000 genomes]
rs2884252	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4719373	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4721252	0.86[ASN][1000 genomes]
rs6955852	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887690	chr7:13591197-13702169	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1026929	chr7:13597929-13716063	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1023839	chr7:13617615-13735946	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv520006	chr7:13641674-13683080	ZNF genes & repeats Enhancers Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv522998	chr7:13641674-13683080	Enhancers Weak transcription ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv887691	chr7:13641674-13685734	Enhancers Weak transcription ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases
7	nsv887692	chr7:13641674-13718969	Enhancers Weak transcription ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases
8	nsv1017756	chr7:13656136-13733606	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1017322	chr7:13661784-13733606	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv887693	chr7:13673538-13718969	Weak transcription Enhancers ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
11	nsv1029362	chr7:13679503-13733647	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13669000-13681400	Weak transcription	NHDF-Ad	bronchial
2	chr7:13679600-13681400	Weak transcription	Fetal Lung	lung

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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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