Variant report

Variant	rs11242992
Chromosome Location	chr6:5130064-5130065
allele	C/T
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: 42 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10484845	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10484846	0.94[MEX][hapmap]
rs12195956	0.94[MEX][hapmap]
rs127124	0.82[CEU][hapmap]
rs17139439	0.94[MEX][hapmap]
rs17139533	0.82[JPT][hapmap]
rs17139551	0.82[JPT][hapmap]
rs2746230	0.84[EUR][1000 genomes]
rs457846	0.80[CEU][hapmap]
rs462749	0.81[CEU][hapmap]
rs464606	0.81[CEU][hapmap]
rs467373	0.88[MEX][hapmap]
rs4959327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4959328	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4960067	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56838333	0.95[ASN][1000 genomes]
rs6597115	0.94[MEX][hapmap]
rs685187	0.84[CEU][hapmap];0.92[CHB][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6914985	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6922265	0.82[JPT][hapmap]
rs6924197	0.82[JPT][hapmap]
rs6937982	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73717664	0.89[ASN][1000 genomes]
rs73717674	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73717675	0.82[EUR][1000 genomes]
rs85204	0.82[CEU][hapmap]
rs9504333	0.93[ASN][1000 genomes]
rs9504338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9504354	0.80[MEX][hapmap]

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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11242992	LYRM4	cis	cerebellum	SCAN

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5101800-5132200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr6:5103200-5132800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:5105200-5131400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:5107800-5132000	Weak transcription	Pancreas	Pancrea
5	chr6:5109200-5130200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr6:5112800-5132600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:5113000-5130400	Weak transcription	Gastric	stomach
8	chr6:5113200-5130400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr6:5113400-5132400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:5123200-5130400	Weak transcription	Left Ventricle	heart
11	chr6:5123400-5132200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:5124800-5133200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr6:5125000-5130600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:5125000-5133200	Weak transcription	Right Ventricle	heart
15	chr6:5125600-5130200	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:5126400-5131800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:5126600-5130200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:5126600-5130400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:5126600-5130400	Weak transcription	Right Atrium	heart
20	chr6:5126600-5133200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:5126600-5134000	Weak transcription	NHEK	skin
22	chr6:5126800-5130400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:5126800-5131600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr6:5126800-5132000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:5126800-5132000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:5126800-5132200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr6:5126800-5132200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:5126800-5132200	Weak transcription	Ovary	ovary
29	chr6:5126800-5132800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:5127000-5130600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr6:5127000-5131400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr6:5127000-5132200	Weak transcription	NHDF-Ad	bronchial
33	chr6:5127200-5132600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:5127600-5130400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:5128400-5130200	Enhancers	Adipose Nuclei	Adipose
36	chr6:5128600-5131000	Enhancers	Spleen	Spleen
37	chr6:5128600-5132400	Weak transcription	Primary B cells from cord blood	blood
38	chr6:5128800-5130600	Weak transcription	Placenta	Placenta
39	chr6:5128800-5132400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr6:5128800-5136200	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr6:5129000-5130800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:5129000-5130800	Strong transcription	Fetal Intestine Small	intestine
43	chr6:5129000-5136800	Weak transcription	Primary T cells from cord blood	blood
44	chr6:5129000-5162000	Weak transcription	K562	blood
45	chr6:5129200-5130600	Enhancers	Lung	lung
46	chr6:5129200-5132600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr6:5129600-5130400	Weak transcription	Fetal Stomach	stomach
48	chr6:5129800-5131800	Weak transcription	Primary B cells from peripheral blood	blood
49	chr6:5129800-5138000	Weak transcription	HepG2	liver
50	chr6:5130000-5130800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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