Variant report

Variant	rs4713368
Chromosome Location	chr6:30757047-30757048
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:30756093..30758891-chr6:30852880..30855209,2	MCF-7	breast:
2	chr6:30756080..30757892-chr6:30785304..30787449,2	MCF-7	breast:
3	chr6:30705811..30713504-chr6:30753060..30768565,33	MCF-7	breast:
4	chr6:30708422..30712193-chr6:30756901..30760196,5	K562	blood:
5	chr6:30750458..30752219-chr6:30756523..30759247,2	MCF-7	breast:
6	chr6:30709229..30711998-chr6:30757042..30758780,2	K562	blood:

Variant related genes	Relation type
ENSG00000137331	Chromatin interaction
ENSG00000137312	Chromatin interaction
ENSG00000272273	Chromatin interaction
ENSG00000204580	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10947091	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10947095	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11758688	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12526481	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12527415	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12527745	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13196596	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13197105	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13197117	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13197227	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13201769	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13201901	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13206009	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13207758	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13210146	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13211218	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13213720	0.90[AFR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16897899	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16897900	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28780116	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28780119	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28894083	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28894084	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28894085	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28894089	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3131042	0.83[ASN][1000 genomes]
rs3131043	0.83[ASN][1000 genomes]
rs3131046	0.83[ASN][1000 genomes]
rs3131051	0.88[ASN][1000 genomes]
rs4711228	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4711229	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4713360	0.89[AFR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4713362	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4713365	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4713366	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4713367	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6900029	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6920124	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7740474	0.82[ASN][1000 genomes]
rs9295912	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9295914	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9461630	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9461631	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9468830	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9468832	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9468833	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	967 gene(s)	inside rSNPs	diseases
5	esv2758041	chr6:30644693-30816319	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
6	esv2759413	chr6:30644693-30816319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
7	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
8	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
9	nsv527226	chr6:30716719-30772378	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	nsv1023695	chr6:30754540-30773349	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30744000-30758000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:30749400-30761200	Weak transcription	Lung	lung
3	chr6:30750400-30761200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:30750600-30758000	Weak transcription	Fetal Heart	heart
5	chr6:30750800-30761200	Weak transcription	Small Intestine	intestine
6	chr6:30750800-30761600	Weak transcription	NHDF-Ad	bronchial
7	chr6:30751000-30769800	Weak transcription	Right Ventricle	heart
8	chr6:30751200-30757800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:30753000-30758000	Enhancers	Dnd41	blood
10	chr6:30753400-30757200	Enhancers	HepG2	liver
11	chr6:30753800-30757600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr6:30754600-30761400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:30755400-30757600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:30755600-30757400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr6:30755600-30757600	Enhancers	Hela-S3	cervix
16	chr6:30755600-30757800	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:30755600-30758000	Enhancers	Primary T cells from cord blood	blood
18	chr6:30755800-30757200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr6:30755800-30757200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:30755800-30757200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr6:30755800-30757400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr6:30755800-30758000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr6:30755800-30758200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:30755800-30762600	Enhancers	Fetal Thymus	thymus
25	chr6:30756000-30757200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:30756000-30757600	Enhancers	K562	blood
27	chr6:30756200-30757400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:30756200-30757400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr6:30756200-30757600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:30756200-30760600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr6:30756200-30761400	Weak transcription	Fetal Stomach	stomach
32	chr6:30756200-30761400	Weak transcription	NH-A	brain
33	chr6:30756400-30757200	Enhancers	Adipose Nuclei	Adipose
34	chr6:30756400-30760400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr6:30756400-30761400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:30756400-30761600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:30756400-30761600	Weak transcription	A549	lung
38	chr6:30756600-30757200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr6:30756600-30757600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:30756600-30757800	Weak transcription	Stomach Mucosa	stomach
41	chr6:30756600-30759800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:30756600-30761000	Weak transcription	Primary B cells from cord blood	blood
43	chr6:30756600-30761200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr6:30756800-30757400	Enhancers	Placenta	Placenta
45	chr6:30756800-30757800	Weak transcription	HMEC	breast
46	chr6:30756800-30758000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr6:30756800-30758400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr6:30756800-30760000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr6:30756800-30761400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:30756800-30761400	Weak transcription	Osteobl	bone

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