Variant report

Variant	rs73727325
Chromosome Location	chr7:150261848-150261849
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10085891	0.81[EUR][1000 genomes]
rs10216102	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10227094	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10239578	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10240209	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10248553	0.82[EUR][1000 genomes]
rs10255487	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10270122	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10273606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11971770	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11975418	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11984138	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12671922	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1317276	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1916027	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2140138	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2140139	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28537284	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28829297	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35890864	0.97[ASN][1000 genomes]
rs4143732	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55653011	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56158089	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57604196	0.85[EUR][1000 genomes]
rs60628216	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6464081	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6959171	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6959264	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6961075	0.92[EUR][1000 genomes]
rs73727323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73727338	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7781704	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7782221	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7787987	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7797456	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7800143	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7802869	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7806724	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs952642	0.94[EUR][1000 genomes]
rs9640279	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[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	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	nsv1025129	chr7:150146593-150266217	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv3395746	chr7:150181141-150300680	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
8	esv3341786	chr7:150220353-150269134	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv16529	chr7:150249312-150312843	Genic enhancers Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
10	esv2758617	chr7:150251949-150463804	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
11	esv2759573	chr7:150251949-150463804	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150259000-150262600	Enhancers	HUVEC	blood vessel
2	chr7:150259800-150262600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
3	chr7:150259800-150263000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:150260000-150262000	Enhancers	Fetal Stomach	stomach
5	chr7:150260400-150262600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:150260400-150262800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
7	chr7:150260400-150264600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:150260600-150262800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr7:150260800-150262200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr7:150260800-150263200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:150260800-150264200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:150260800-150265000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:150261000-150262200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:150261200-150262400	Enhancers	Fetal Brain Female	brain
15	chr7:150261200-150262600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:150261400-150262000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:150261400-150262000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:150261400-150262000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:150261400-150262400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr7:150261600-150262000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:150261600-150262000	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr7:150261600-150262200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr7:150261600-150263000	Enhancers	Primary T cells from cord blood	blood
24	chr7:150261600-150263200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr7:150261600-150263600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr7:150261600-150263800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:150261800-150262600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr7:150261800-150263600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:150261800-150263800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:150261800-150263800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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