Variant report

Variant	rs458743
Chromosome Location	chr6:5129404-5129405
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:5120295..5122743-chr6:5128225..5130886,2	K562	blood:
2	chr6:5120935..5125341-chr6:5126554..5131441,5	K562	blood:
3	chr6:5127863..5130262-chr6:5130586..5132719,2	K562	blood:
4	chr6:5128862..5130386-chr6:5130746..5132624,2	MCF-7	breast:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1571564	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs175596	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs200844	0.82[AMR][1000 genomes]
rs200859	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs200860	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs200862	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs200866	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs200867	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs200868	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs200869	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs200870	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2143693	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2746239	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs373696	0.83[ASN][1000 genomes]
rs374117	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs378359	0.82[CEU][hapmap]
rs379508	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs379511	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs381472	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs385481	0.82[CEU][hapmap]
rs388597	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs392847	0.81[ASN][1000 genomes]
rs393055	1.00[ASN][1000 genomes]
rs393300	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs393332	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs393628	0.82[CEU][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs399120	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs411483	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs414986	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs417629	0.81[ASN][1000 genomes]
rs424006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs434706	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs450176	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs458108	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs458283	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460416	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs461465	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs462327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs462487	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs465453	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs465481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs466285	0.88[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4960069	1.00[JPT][hapmap]
rs52401	0.80[ASN][1000 genomes]
rs620360	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6597117	1.00[JPT][hapmap]
rs7752848	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs7766717	1.00[JPT][hapmap]
rs9405257	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv462622	chr6:4904380-5172009	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv600871	chr6:4904380-5172009	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1017380	chr6:5007870-5152551	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1034681	chr6:5070351-5387176	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
8	nsv538113	chr6:5070351-5387176	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1018152	chr6:5077025-5387176	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
10	nsv600873	chr6:5089278-5400658	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1017821	chr6:5114609-5213200	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
12	nsv538114	chr6:5114609-5213200	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
13	nsv5179	chr6:5121824-5167027	Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5099000-5130000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:5101800-5132200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:5103200-5132800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:5105200-5131400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:5107800-5132000	Weak transcription	Pancreas	Pancrea
6	chr6:5109200-5130200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:5112800-5132600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:5113000-5130400	Weak transcription	Gastric	stomach
9	chr6:5113200-5130400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:5113400-5132400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr6:5123200-5130400	Weak transcription	Left Ventricle	heart
12	chr6:5123400-5132200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:5124800-5133200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:5125000-5130600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:5125000-5133200	Weak transcription	Right Ventricle	heart
16	chr6:5125600-5130200	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:5126400-5131800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:5126600-5130200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:5126600-5130400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:5126600-5130400	Weak transcription	Right Atrium	heart
21	chr6:5126600-5133200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:5126600-5134000	Weak transcription	NHEK	skin
23	chr6:5126800-5130000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:5126800-5130000	Weak transcription	Fetal Heart	heart
25	chr6:5126800-5130400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:5126800-5131600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr6:5126800-5132000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr6:5126800-5132000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:5126800-5132200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr6:5126800-5132200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:5126800-5132200	Weak transcription	Ovary	ovary
32	chr6:5126800-5132800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr6:5127000-5130600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr6:5127000-5131400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr6:5127000-5132200	Weak transcription	NHDF-Ad	bronchial
36	chr6:5127200-5132600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:5127600-5130400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:5128200-5129600	Enhancers	Fetal Thymus	thymus
39	chr6:5128400-5129800	Enhancers	Primary B cells from peripheral blood	blood
40	chr6:5128400-5130200	Enhancers	Adipose Nuclei	Adipose
41	chr6:5128600-5131000	Enhancers	Spleen	Spleen
42	chr6:5128600-5132400	Weak transcription	Primary B cells from cord blood	blood
43	chr6:5128800-5130600	Weak transcription	Placenta	Placenta
44	chr6:5128800-5132400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr6:5128800-5136200	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr6:5129000-5129600	Strong transcription	Fetal Stomach	stomach
47	chr6:5129000-5130800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:5129000-5130800	Strong transcription	Fetal Intestine Small	intestine
49	chr6:5129000-5136800	Weak transcription	Primary T cells from cord blood	blood
50	chr6:5129000-5162000	Weak transcription	K562	blood

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