Variant report

Variant	rs9591178
Chromosome Location	chr13:49134650-49134651
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1547660	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1926595	1.00[ASN][1000 genomes]
rs1926596	0.91[ASN][1000 genomes]
rs1926597	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198564	0.85[ASN][1000 genomes]
rs198568	0.88[ASN][1000 genomes]
rs198571	0.88[ASN][1000 genomes]
rs198574	0.88[ASN][1000 genomes]
rs198575	0.88[ASN][1000 genomes]
rs198576	0.88[ASN][1000 genomes]
rs198577	0.88[ASN][1000 genomes]
rs2274400	0.91[ASN][1000 genomes]
rs28414460	0.91[ASN][1000 genomes]
rs28646083	0.91[ASN][1000 genomes]
rs28674973	0.84[ASN][1000 genomes]
rs2897587	0.88[AFR][1000 genomes]
rs3092898	0.88[ASN][1000 genomes]
rs3751380	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs398158	0.85[ASN][1000 genomes]
rs403390	0.88[ASN][1000 genomes]
rs61074776	1.00[ASN][1000 genomes]
rs6561448	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6561457	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6561461	1.00[ASN][1000 genomes]
rs7325962	0.83[ASN][1000 genomes]
rs7329039	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7329865	0.84[ASN][1000 genomes]
rs73486867	1.00[ASN][1000 genomes]
rs73495016	0.88[ASN][1000 genomes]
rs7985825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7987935	0.91[ASN][1000 genomes]
rs7992129	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7995216	0.97[ASN][1000 genomes]
rs7996186	0.91[ASN][1000 genomes]
rs7996402	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7998781	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8001241	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8002565	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9316385	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9316401	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9331959	0.91[ASN][1000 genomes]
rs9331965	0.88[ASN][1000 genomes]
rs9331973	0.91[ASN][1000 genomes]
rs9332054	0.83[ASN][1000 genomes]
rs9591172	1.00[ASN][1000 genomes]
rs9591177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9595929	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832602	chr13:49003159-49167781	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv1041275	chr13:49045566-49242357	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers 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	14 gene(s)	inside rSNPs	diseases
3	nsv541769	chr13:49045566-49242357	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
5	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv455881	chr13:49134412-49169570	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv561591	chr13:49134412-49169570	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49132200-49135000	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr13:49132200-49135000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr13:49133200-49134800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:49133400-49135600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:49133600-49135000	Enhancers	Dnd41	blood
6	chr13:49133600-49135000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr13:49133600-49136000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr13:49133800-49135800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr13:49134000-49135600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr13:49134200-49136200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:49134200-49136200	Weak transcription	HSMM	muscle
12	chr13:49134200-49137400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr13:49134400-49135600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr13:49134400-49136200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr13:49134400-49136200	Weak transcription	HMEC	breast
16	chr13:49134400-49137600	Enhancers	Primary T cells fromperipheralblood	blood
17	chr13:49134600-49135600	Weak transcription	K562	blood
18	chr13:49134600-49136400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr13:49134600-49138000	Weak transcription	Osteobl	bone

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