Variant report

Variant	rs13422994
Chromosome Location	chr2:231128179-231128180
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10164566	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10177685	0.81[ASN][1000 genomes]
rs10200874	0.81[ASN][1000 genomes]
rs10498245	0.81[ASN][1000 genomes]
rs12472020	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12477360	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13395371	0.81[ASN][1000 genomes]
rs16826952	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1863674	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1863677	0.81[ASN][1000 genomes]
rs2081713	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2114588	0.81[ASN][1000 genomes]
rs2114590	0.81[ASN][1000 genomes]
rs2162481	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2396741	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34839676	0.81[ASN][1000 genomes]
rs3769841	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3769842	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3769843	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3769844	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3769846	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3813464	0.81[ASN][1000 genomes]
rs3820975	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3829782	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4343458	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4972943	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4972945	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4973302	0.88[EUR][1000 genomes]
rs4973304	0.81[ASN][1000 genomes]
rs4973305	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4973306	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57003673	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57402789	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59020873	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59805999	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61575136	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62191186	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191188	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191189	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62191191	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191192	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191193	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191196	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191197	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191199	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191200	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191201	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62191202	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62192161	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62193107	0.88[EUR][1000 genomes]
rs62193138	0.88[EUR][1000 genomes]
rs62193139	0.88[EUR][1000 genomes]
rs62193140	0.88[EUR][1000 genomes]
rs62193141	0.88[EUR][1000 genomes]
rs62193142	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62193143	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62193147	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7576496	0.88[EUR][1000 genomes]
rs7591582	0.88[EUR][1000 genomes]
rs9989792	0.81[ASN][1000 genomes]
rs9989808	0.81[ASN][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	nsv1001562	chr2:230862717-231187043	Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv536156	chr2:230862717-231187043	Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv498047	chr2:230951712-231250489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv869834	chr2:231045013-231139827	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats 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	4 gene(s)	inside rSNPs	diseases
5	nsv998291	chr2:231045388-231136278	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231090200-231170000	Weak transcription	Spleen	Spleen
2	chr2:231119200-231141200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr2:231120600-231134200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr2:231122800-231129800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:231125400-231136800	Strong transcription	Primary B cells from cord blood	blood
6	chr2:231125600-231128200	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr2:231125600-231128600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr2:231125600-231128600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr2:231125800-231128600	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr2:231126000-231128600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr2:231126400-231128200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr2:231127200-231128400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr2:231127200-231130000	Weak transcription	GM12878-XiMat	blood
14	chr2:231127400-231129200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr2:231127400-231129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:231127600-231128200	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr2:231127600-231130200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:231127800-231135400	Weak transcription	Primary T cells from cord blood	blood
19	chr2:231128000-231128600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr2:231128000-231129400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr2:231128000-231131000	Strong transcription	Primary B cells from peripheral blood	blood

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