Variant report

Variant	rs73410234
Chromosome Location	chr6:36593184-36593185
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:10)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:10 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MXI1	chr6:36592618-36593441	IMR90	lung:	n/a	n/a
2	FOXA1	chr6:36592887-36593232	HepG2	liver:	n/a	n/a
3	FOXA1	chr6:36592934-36593200	ECC-1	luminal epithelium:	n/a	n/a
4	FOXA2	chr6:36592863-36593274	A549	lung:	n/a	n/a
5	FOXA2	chr6:36592899-36593274	A549	lung:	n/a	n/a
6	CTCF	chr6:36593180-36593330	HCPEpiC	choroid plexus:	n/a	n/a
7	RAD21	chr6:36592912-36593213	IMR90	lung:	n/a	n/a
8	MAX	chr6:36592905-36593429	MCF-7	breast:	n/a	chr6:36593015-36593024 chr6:36593191-36593202
9	FOXA1	chr6:36592769-36593187	HepG2	liver:	n/a	n/a
10	FOXA2	chr6:36592922-36593190	HepG2	liver:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36591678..36593501-chr6:36719178..36722554,3	MCF-7	breast:
2	chr6:36588192..36591183-chr6:36591330..36594102,4	MCF-7	breast:
3	chr6:36590968..36593681-chr6:36692597..36695208,2	MCF-7	breast:
4	chr6:36593028..36595408-chr6:36598943..36601899,2	MCF-7	breast:
5	chr6:36589971..36596625-chr6:36645571..36650576,10	K562	blood:
6	chr6:36591755..36593263-chr6:36601284..36603461,2	MCF-7	breast:
7	chr6:36589213..36595227-chr6:36645571..36651666,9	K562	blood:
8	chr6:36560666..36565212-chr6:36591951..36596292,5	K562	blood:
9	chr6:36592594..36594352-chr6:36598333..36600462,2	K562	blood:
10	chr6:36581224..36597272-chr6:36642199..36659412,120	MCF-7	breast:
11	chr6:36592740..36594908-chr6:36630647..36632987,2	MCF-7	breast:
12	chr6:36591713..36594218-chr6:36617666..36619384,2	MCF-7	breast:
13	chr6:36581748..36603537-chr6:36641861..36652365,77	MCF-7	breast:

No data

Variant related genes	Relation type
MIR3925	TF binding region
ENSG00000112081	Chromatin interaction
ENSG00000263894	Chromatin interaction
ENSG00000124762	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11552549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17553386	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3087654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56799886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56814071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56845418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56900755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56900950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58073599	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59274016	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59569857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59715484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61631302	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62402215	0.86[ASN][1000 genomes]
rs73408319	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408346	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408347	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408354	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408356	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408360	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73408367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408370	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408373	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408391	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408400	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410218	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410228	0.91[AFR][1000 genomes]
rs73410230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410237	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410240	0.92[EUR][1000 genomes]
rs73410246	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885806	chr6:36349890-36621178	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
2	nsv1031191	chr6:36588974-36718015	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv538201	chr6:36588974-36718015	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36577400-36595200	Weak transcription	Psoas Muscle	Psoas
2	chr6:36577800-36595200	Weak transcription	Small Intestine	intestine
3	chr6:36580200-36599200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:36581400-36604400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr6:36582200-36595400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:36582800-36610800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:36587000-36597000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:36588800-36595400	Enhancers	Duodenum Mucosa	Duodenum
9	chr6:36590200-36593400	Enhancers	Adipose Nuclei	Adipose
10	chr6:36590400-36593600	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr6:36590400-36593600	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr6:36590600-36593200	Enhancers	Colonic Mucosa	Colon
13	chr6:36590600-36593400	Enhancers	Fetal Intestine Large	intestine
14	chr6:36590600-36593400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr6:36590600-36593600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:36590600-36596000	Enhancers	Fetal Muscle Leg	muscle
17	chr6:36590800-36593200	Enhancers	Liver	Liver
18	chr6:36590800-36593200	Enhancers	Fetal Intestine Small	intestine
19	chr6:36590800-36593400	Enhancers	Stomach Mucosa	stomach
20	chr6:36590800-36593600	Enhancers	Colon Smooth Muscle	Colon
21	chr6:36590800-36593600	Enhancers	Fetal Muscle Trunk	muscle
22	chr6:36590800-36593600	Enhancers	Pancreas	Pancrea
23	chr6:36590800-36593800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:36590800-36593800	Enhancers	Hela-S3	cervix
25	chr6:36591000-36593200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:36591000-36593600	Enhancers	Fetal Kidney	kidney
27	chr6:36591000-36595800	Enhancers	Ovary	ovary
28	chr6:36591000-36596000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:36591200-36593600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr6:36591200-36595200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:36591200-36595600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:36591200-36596000	Enhancers	Fetal Lung	lung
33	chr6:36591400-36593200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr6:36591400-36593600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr6:36591600-36593200	Weak transcription	Thymus	Thymus
36	chr6:36591600-36594200	Weak transcription	HUVEC	blood vessel
37	chr6:36591600-36595400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:36591600-36597000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:36591800-36593200	Weak transcription	Brain Substantia Nigra	brain
40	chr6:36591800-36595400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:36592000-36593200	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr6:36592000-36594600	Weak transcription	Lung	lung
43	chr6:36592000-36595200	Weak transcription	Placenta	Placenta
44	chr6:36592000-36595200	Weak transcription	Left Ventricle	heart
45	chr6:36592200-36593200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr6:36592200-36593200	Weak transcription	Brain Anterior Caudate	brain
47	chr6:36592200-36593200	Weak transcription	Fetal Thymus	thymus
48	chr6:36592200-36593400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:36592200-36593400	Bivalent Enhancer	HepG2	liver
50	chr6:36592200-36593600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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