Variant report

Variant	rs7250673
Chromosome Location	chr19:19968880-19968881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10401290	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10401847	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10401908	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10402267	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10405029	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10406942	0.91[AMR][1000 genomes]
rs10407581	1.00[EUR][1000 genomes]
rs10408499	0.84[AMR][1000 genomes]
rs10408890	1.00[EUR][1000 genomes]
rs10409568	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10411668	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10412298	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10414667	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10416020	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10419073	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10423312	1.00[EUR][1000 genomes]
rs10423574	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10423992	1.00[EUR][1000 genomes]
rs10425214	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11878325	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11879946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11880495	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11880971	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11880972	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11880975	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11881233	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11881507	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11882779	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11882889	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13346878	1.00[EUR][1000 genomes]
rs16996376	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28437283	1.00[EUR][1000 genomes]
rs28622316	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28655627	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28668259	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28696819	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28698719	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45447205	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55870166	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56413930	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57018770	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57405289	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57691007	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59586774	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60287284	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7251735	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73526738	1.00[EUR][1000 genomes]
rs73526768	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73528913	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73528956	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73923028	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73925538	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv911314	chr19:19866371-20021046	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv911315	chr19:19872093-20021046	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv911316	chr19:19890450-20021046	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv961192	chr19:19906394-20083740	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	esv3413756	chr19:19936066-20072059	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv3380276	chr19:19936583-20073601	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1066792	chr19:19940585-20000701	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	esv3429980	chr19:19943721-20102072	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
14	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19959200-19971200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:19965200-19970800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr19:19966600-19970200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:19967000-19969400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr19:19967000-19969600	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr19:19967200-19969400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr19:19968600-19971400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr19:19968800-19969000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr19:19968800-19969200	Strong transcription	H9 Cell Line	embryonic stem cell

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