Variant report

Variant	rs59183825
Chromosome Location	chr6:34568813-34568814
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34508607..34511346-chr6:34567639..34570139,2	K562	blood:
2	chr6:34563477..34566379-chr6:34567345..34568869,2	K562	blood:
3	chr6:34550788..34556388-chr6:34565460..34570894,5	K562	blood:
4	chr6:34202035..34203669-chr6:34568608..34571560,2	K562	blood:
5	chr6:34567678..34570599-chr6:34570819..34574563,3	K562	blood:
6	chr6:34521513..34524596-chr6:34566930..34571900,4	MCF-7	breast:
7	chr6:34559251..34563150-chr6:34565223..34569696,5	K562	blood:

Variant related genes	Relation type
ENSG00000124664	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs12111029	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57048285	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57106758	1.00[ASN][1000 genomes]
rs57157056	1.00[EUR][1000 genomes]
rs58971485	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59191826	0.91[AFR][1000 genomes]
rs59240548	1.00[ASN][1000 genomes]
rs60220209	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61316456	1.00[EUR][1000 genomes]
rs61510762	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901047	1.00[EUR][1000 genomes]
rs6906562	1.00[EUR][1000 genomes]
rs6908049	1.00[EUR][1000 genomes]
rs6913199	1.00[EUR][1000 genomes]
rs6913396	1.00[EUR][1000 genomes]
rs6913723	1.00[ASN][1000 genomes]
rs6919218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6921954	1.00[EUR][1000 genomes]
rs6924259	1.00[ASN][1000 genomes]
rs6931073	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6931985	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6936924	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6938501	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6939293	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6939783	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73407800	1.00[EUR][1000 genomes]
rs73409960	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409969	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409978	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409980	1.00[EUR][1000 genomes]
rs73409982	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409995	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409996	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410000	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73411915	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73411933	1.00[EUR][1000 genomes]
rs73411935	1.00[ASN][1000 genomes]
rs73411944	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73411950	1.00[EUR][1000 genomes]
rs73411956	1.00[ASN][1000 genomes]
rs73411957	1.00[ASN][1000 genomes]
rs73411961	1.00[EUR][1000 genomes]
rs73411971	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73411982	1.00[ASN][1000 genomes]
rs73411992	1.00[ASN][1000 genomes]
rs73411995	1.00[ASN][1000 genomes]
rs73411997	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73413803	1.00[EUR][1000 genomes]
rs73413804	1.00[ASN][1000 genomes]
rs73413808	1.00[ASN][1000 genomes]
rs73413811	1.00[ASN][1000 genomes]
rs73413812	1.00[ASN][1000 genomes]
rs73413815	1.00[ASN][1000 genomes]
rs73413824	1.00[ASN][1000 genomes]
rs73413828	1.00[ASN][1000 genomes]
rs73413843	1.00[ASN][1000 genomes]
rs73413845	1.00[ASN][1000 genomes]
rs73413847	1.00[ASN][1000 genomes]
rs73413854	1.00[ASN][1000 genomes]
rs73413867	1.00[EUR][1000 genomes]
rs73413869	1.00[ASN][1000 genomes]
rs73413870	1.00[ASN][1000 genomes]
rs73413875	1.00[ASN][1000 genomes]
rs73413879	1.00[ASN][1000 genomes]
rs73413885	1.00[ASN][1000 genomes]
rs73746653	1.00[ASN][1000 genomes]
rs7738897	1.00[EUR][1000 genomes]
rs7739387	1.00[EUR][1000 genomes]
rs7742598	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7745409	1.00[EUR][1000 genomes]
rs7748850	1.00[EUR][1000 genomes]
rs7762266	1.00[EUR][1000 genomes]
rs7762752	1.00[ASN][1000 genomes]
rs7766367	1.00[EUR][1000 genomes]
rs7766657	1.00[ASN][1000 genomes]
rs7772931	1.00[EUR][1000 genomes]
rs9942450	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS 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	49 gene(s)	inside rSNPs	diseases
6	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	38 gene(s)	inside rSNPs	diseases
7	nsv885792	chr6:34507311-34607958	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv823667	chr6:34533015-34592524	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv818410	chr6:34538544-34579431	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
11	nsv830640	chr6:34542489-34714677	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers 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 target site	24 gene(s)	inside rSNPs	diseases
12	nsv885794	chr6:34561585-34673149	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1032557	chr6:34565802-34802008	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
14	nsv538196	chr6:34565802-34802008	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	esv2763967	chr6:34566255-34925463	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34553400-34570000	Weak transcription	NH-A	brain
2	chr6:34554000-34573600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:34554600-34577200	Weak transcription	HUVEC	blood vessel
4	chr6:34555400-34574200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:34555600-34569200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:34556200-34612200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:34557200-34573600	Weak transcription	Colonic Mucosa	Colon
8	chr6:34557400-34612400	Weak transcription	Fetal Kidney	kidney
9	chr6:34557600-34569000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:34557600-34569200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr6:34557600-34569600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:34557600-34569600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:34557600-34573200	Weak transcription	Spleen	Spleen
14	chr6:34557600-34573400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:34558000-34570000	Weak transcription	Fetal Intestine Large	intestine
16	chr6:34558000-34573400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:34558000-34573400	Weak transcription	Placenta	Placenta
18	chr6:34558200-34571600	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr6:34558400-34577200	Weak transcription	Hela-S3	cervix
20	chr6:34558600-34569000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:34558600-34570400	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:34560200-34573400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr6:34560400-34578600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr6:34560600-34570400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr6:34560800-34572200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:34561600-34575400	Strong transcription	Primary T cells from cord blood	blood
27	chr6:34562000-34569600	Weak transcription	HSMM	muscle
28	chr6:34562600-34570600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr6:34562600-34585200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:34563800-34569200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:34563800-34570000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:34563800-34579000	Weak transcription	HMEC	breast
33	chr6:34564000-34569000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:34564000-34578000	Weak transcription	NHDF-Ad	bronchial
35	chr6:34564200-34569000	Weak transcription	Fetal Intestine Small	intestine
36	chr6:34564200-34569600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:34564200-34570200	Weak transcription	NHLF	lung
38	chr6:34564600-34569600	Weak transcription	HSMMtube	muscle
39	chr6:34564800-34569200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:34564800-34571000	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr6:34565000-34571000	Enhancers	Adipose Nuclei	Adipose
42	chr6:34565000-34571800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr6:34565200-34570800	Enhancers	Brain Angular Gyrus	brain
44	chr6:34565200-34570800	Enhancers	Ovary	ovary
45	chr6:34565200-34572400	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr6:34565600-34574200	Weak transcription	Esophagus	oesophagus
47	chr6:34565600-34576000	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr6:34565800-34571000	Enhancers	Fetal Heart	heart
49	chr6:34566000-34569000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:34566000-34573600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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