Variant report

Variant	rs6476437
Chromosome Location	chr9:3421997-3421998
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs13285649	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13301035	1.00[JPT][hapmap]
rs6476436	0.80[AMR][1000 genomes]
rs7021039	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[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	nsv1032921	chr9:3139007-3502815	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv539940	chr9:3139007-3502815	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv531566	chr9:3288211-3545454	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv892089	chr9:3290569-3578094	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv916259	chr9:3308176-4296711	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv1034280	chr9:3319718-3491987	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv539942	chr9:3319718-3491987	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1028815	chr9:3319718-3584455	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv613147	chr9:3368111-3440355	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv892090	chr9:3391364-3496660	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3382200-3425000	Weak transcription	Aorta	Aorta
2	chr9:3387200-3433800	Weak transcription	Pancreas	Pancrea
3	chr9:3398800-3423400	Weak transcription	Primary T cells from cord blood	blood
4	chr9:3398800-3437200	Weak transcription	Primary B cells from cord blood	blood
5	chr9:3402400-3425000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:3410800-3425000	Weak transcription	Brain Germinal Matrix	brain
7	chr9:3411000-3425400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr9:3412000-3434600	Weak transcription	Ovary	ovary
9	chr9:3414200-3426200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:3414400-3424800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:3416400-3425000	Weak transcription	Fetal Intestine Small	intestine
12	chr9:3416400-3425000	Weak transcription	Fetal Lung	lung
13	chr9:3418400-3425000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr9:3419000-3437000	Weak transcription	Brain Substantia Nigra	brain
15	chr9:3420200-3426400	Weak transcription	Left Ventricle	heart
16	chr9:3420200-3427800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:3420400-3425000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:3420600-3425000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:3420800-3422000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:3420800-3422000	Weak transcription	Fetal Heart	heart
21	chr9:3421200-3423400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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