Variant report

Variant	rs61047660
Chromosome Location	chr6:121604516-121604517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1273719	0.89[ASN][1000 genomes]
rs17083186	0.89[ASN][1000 genomes]
rs17083373	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17083415	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17083440	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17154	0.95[ASN][1000 genomes]
rs2133990	0.95[ASN][1000 genomes]
rs2186097	0.92[ASN][1000 genomes]
rs2892765	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4072142	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4132315	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4305755	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4371872	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4584021	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55731091	0.89[ASN][1000 genomes]
rs55799213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55975505	0.89[AFR][1000 genomes]
rs55983388	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56000113	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56927912	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58124381	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61293964	0.95[ASN][1000 genomes]
rs6903467	0.95[ASN][1000 genomes]
rs6919916	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6920055	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6920884	0.92[ASN][1000 genomes]
rs6925413	0.95[ASN][1000 genomes]
rs6941089	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73526695	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73528541	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73768932	0.95[ASN][1000 genomes]
rs73768938	0.95[ASN][1000 genomes]
rs7451033	0.95[ASN][1000 genomes]
rs7741356	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7742071	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7743455	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7744891	0.95[ASN][1000 genomes]
rs7749984	0.95[ASN][1000 genomes]
rs7751636	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7755977	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7757350	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7759798	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7761551	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7765795	0.95[ASN][1000 genomes]
rs7767417	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7768813	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9490148	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023384	chr6:121235867-121683448	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv530527	chr6:121298528-121789855	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv830789	chr6:121581450-121732320	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1017944	chr6:121600538-121644362	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121575000-121606400	Weak transcription	NH-A	brain
2	chr6:121585400-121614200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:121585600-121625000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:121586400-121655000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr6:121586600-121613000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:121588200-121616800	Weak transcription	Primary T cells from cord blood	blood
7	chr6:121588400-121655200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:121588600-121612000	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr6:121588600-121617600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:121588800-121642000	Weak transcription	Left Ventricle	heart
11	chr6:121589000-121632800	Weak transcription	Fetal Lung	lung
12	chr6:121589000-121635200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr6:121589000-121637600	Weak transcription	Ovary	ovary
14	chr6:121589000-121654200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:121589200-121605200	Weak transcription	Dnd41	blood
16	chr6:121589200-121622400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:121589200-121630000	Weak transcription	Fetal Intestine Large	intestine
18	chr6:121589200-121631800	Weak transcription	Fetal Intestine Small	intestine
19	chr6:121589200-121655000	Weak transcription	Fetal Stomach	stomach
20	chr6:121589400-121612400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr6:121589600-121615600	Weak transcription	Fetal Brain Female	brain
22	chr6:121590200-121630800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:121593800-121605800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:121594000-121606200	Weak transcription	NHLF	lung
25	chr6:121594200-121654800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:121594600-121622400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:121595400-121616600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr6:121596000-121605400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:121596600-121605200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:121597600-121617200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr6:121598000-121622400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:121598200-121612200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr6:121599400-121612800	Weak transcription	Brain Substantia Nigra	brain
34	chr6:121601600-121635200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr6:121602400-121606400	Weak transcription	HSMM	muscle
36	chr6:121602600-121637800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:121603000-121632600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr6:121603400-121604800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:121604000-121604800	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr6:121604000-121605800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:121604000-121645200	Weak transcription	Fetal Kidney	kidney
42	chr6:121604400-121642000	Weak transcription	Primary B cells from cord blood	blood

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