Variant report

Variant	rs4397218
Chromosome Location	chr6:24807556-24807557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10806993	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10806994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946728	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10946729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946730	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4282395	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4360127	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4391258	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4504470	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4509111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4513786	0.81[AMR][1000 genomes]
rs4712856	0.81[AMR][1000 genomes]
rs6456636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912790	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6931983	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6931984	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6932132	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6932829	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6932875	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6933295	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7751848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358804	0.81[AMR][1000 genomes]
rs9379691	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9379692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9393587	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9467322	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830609	chr6:24712086-24896647	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv5227	chr6:24774149-24824012	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv508396	chr6:24779648-24846309	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24776800-24807600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:24777000-24808000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:24777000-24809400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:24777000-24811600	Weak transcription	Brain Hippocampus Middle	brain
5	chr6:24777000-24847600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:24777000-24859600	Weak transcription	Psoas Muscle	Psoas
7	chr6:24788000-24810200	Weak transcription	Left Ventricle	heart
8	chr6:24788000-24832000	Weak transcription	Brain Substantia Nigra	brain
9	chr6:24788800-24848200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:24789200-24842600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:24789400-24807800	Weak transcription	Dnd41	blood
12	chr6:24798200-24827400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:24798200-24841200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr6:24800000-24843200	Weak transcription	Liver	Liver
15	chr6:24800200-24809400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:24800400-24821800	Weak transcription	Fetal Heart	heart
17	chr6:24800800-24811800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr6:24800800-24811800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:24801000-24812000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr6:24801200-24811800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr6:24801200-24812000	Strong transcription	Primary B cells from peripheral blood	blood
22	chr6:24801400-24811800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:24801600-24811200	Strong transcription	Primary T cells from cord blood	blood
24	chr6:24802000-24810600	Strong transcription	Primary B cells from cord blood	blood
25	chr6:24802000-24811000	Strong transcription	Primary hematopoietic stem cells	blood
26	chr6:24802000-24811000	Strong transcription	Fetal Thymus	thymus
27	chr6:24802000-24811600	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr6:24802000-24811800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr6:24802000-24811800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:24802000-24812000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:24802400-24811600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
32	chr6:24802400-24811600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:24802400-24811800	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr6:24802400-24811800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr6:24802600-24810600	Strong transcription	Thymus	Thymus
36	chr6:24802600-24812000	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr6:24802600-24834200	Weak transcription	HSMM	muscle
38	chr6:24802800-24827400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr6:24803200-24811000	Strong transcription	HSMMtube	muscle
40	chr6:24803400-24809000	Weak transcription	Pancreas	Pancrea
41	chr6:24803400-24810200	Weak transcription	Lung	lung
42	chr6:24803400-24817800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr6:24803400-24827400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:24803600-24807800	Weak transcription	NHDF-Ad	bronchial
45	chr6:24804000-24809400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr6:24804200-24810000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:24804600-24809200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr6:24804800-24810000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:24804800-24811200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr6:24804800-24858200	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links