Variant report

Variant	rs2985171
Chromosome Location	chr13:38237872-38237873
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1298657	1.00[AMR][1000 genomes]
rs1333355	1.00[AMR][1000 genomes]
rs1333356	1.00[AMR][1000 genomes]
rs1333357	1.00[AMR][1000 genomes]
rs1333363	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs1413000	1.00[AMR][1000 genomes]
rs1475245	1.00[AMR][1000 genomes]
rs1570610	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs1577008	1.00[AMR][1000 genomes]
rs17056136	1.00[CEU][hapmap]
rs17056209	1.00[CEU][hapmap]
rs1924282	1.00[AMR][1000 genomes]
rs1924284	1.00[AMR][1000 genomes]
rs1924287	1.00[AMR][1000 genomes]
rs1924294	1.00[AMR][1000 genomes]
rs1924297	1.00[AMR][1000 genomes]
rs1924305	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1924308	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1981057	1.00[AMR][1000 genomes]
rs2031272	1.00[AMR][1000 genomes]
rs2031273	1.00[AMR][1000 genomes]
rs2181773	1.00[CEU][hapmap]
rs2957213	1.00[AMR][1000 genomes]
rs2985157	1.00[AMR][1000 genomes]
rs2985158	1.00[AMR][1000 genomes]
rs2985166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2985172	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4343144	1.00[AMR][1000 genomes]
rs4418936	1.00[AMR][1000 genomes]
rs4480663	1.00[AMR][1000 genomes]
rs4595666	1.00[AMR][1000 genomes]
rs4943530	1.00[AMR][1000 genomes]
rs545636	1.00[AMR][1000 genomes]
rs604068	1.00[CEU][hapmap]
rs615491	1.00[AMR][1000 genomes]
rs6563568	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs662478	1.00[AMR][1000 genomes]
rs669862	1.00[AMR][1000 genomes]
rs7334202	1.00[AMR][1000 genomes]
rs7984439	1.00[AMR][1000 genomes]
rs7989413	1.00[AMR][1000 genomes]
rs7990804	1.00[AMR][1000 genomes]
rs8002347	1.00[AMR][1000 genomes]
rs817616	1.00[AMR][1000 genomes]
rs860144	1.00[AMR][1000 genomes]
rs912386	1.00[AMR][1000 genomes]
rs9285117	1.00[AMR][1000 genomes]
rs9547981	1.00[AMR][1000 genomes]
rs9547989	1.00[AMR][1000 genomes]
rs9548002	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9548019	1.00[AMR][1000 genomes]
rs959269	1.00[AMR][1000 genomes]
rs9603229	1.00[AMR][1000 genomes]
rs963953	1.00[CEU][hapmap]

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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1045716	chr13:37952062-38394595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38211400-38275600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr13:38221600-38239600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr13:38221800-38239400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr13:38225600-38246600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:38228000-38238200	Weak transcription	Left Ventricle	heart
6	chr13:38231000-38241200	Weak transcription	Aorta	Aorta
7	chr13:38231800-38255000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:38232600-38239600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:38233200-38239800	Weak transcription	NHLF	lung
10	chr13:38233400-38239200	Weak transcription	HUVEC	blood vessel
11	chr13:38233600-38239800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:38233800-38239600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:38234000-38256000	Weak transcription	Ovary	ovary
14	chr13:38236800-38238000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr13:38236800-38238200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:38236800-38238200	Strong transcription	Osteobl	bone
17	chr13:38237200-38239600	Weak transcription	NHDF-Ad	bronchial
18	chr13:38237800-38238000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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