Variant report

Variant	rs2031272
Chromosome Location	chr13:38214792-38214793
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:38214540..38215112-chr13:39489657..39490374,2	MCF-7	breast:
2	chr13:38214419..38215258-chr13:38518999..38519682,2	MCF-7	breast:
3	chr13:38214466..38215276-chr13:38619175..38620143,2	MCF-7	breast:
4	chr13:38214293..38215171-chr13:38619746..38620556,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1298657	1.00[AMR][1000 genomes]
rs1333355	1.00[AMR][1000 genomes]
rs1333356	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs1333357	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs1333363	1.00[AMR][1000 genomes]
rs1413000	1.00[AMR][1000 genomes]
rs1475245	1.00[AMR][1000 genomes]
rs1570610	1.00[AMR][1000 genomes]
rs1577008	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs1924282	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs1924284	0.83[YRI][hapmap];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[AMR][1000 genomes]
rs1924308	1.00[AMR][1000 genomes]
rs1981057	1.00[AMR][1000 genomes]
rs2031273	1.00[AMR][1000 genomes]
rs2039434	0.83[YRI][hapmap]
rs2957213	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs2985157	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs2985158	1.00[AMR][1000 genomes]
rs2985166	1.00[AMR][1000 genomes]
rs2985171	1.00[AMR][1000 genomes]
rs2985172	1.00[AMR][1000 genomes]
rs4343144	0.83[YRI][hapmap];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]
rs615491	1.00[AMR][1000 genomes]
rs6563568	1.00[AMR][1000 genomes]
rs662478	1.00[AMR][1000 genomes]
rs669862	1.00[AMR][1000 genomes]
rs7329237	0.83[YRI][hapmap]
rs7334202	1.00[AMR][1000 genomes]
rs7984439	1.00[AMR][1000 genomes]
rs7989413	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs7990804	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs8002347	1.00[AMR][1000 genomes]
rs912386	1.00[AMR][1000 genomes]
rs9285117	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs9547981	1.00[AMR][1000 genomes]
rs9547989	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9547990	0.80[AFR][1000 genomes]
rs9548002	1.00[AMR][1000 genomes]
rs9548019	1.00[AMR][1000 genomes]
rs959269	1.00[AMR][1000 genomes]
rs9603229	1.00[AMR][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	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:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38204800-38215400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:38207400-38215000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr13:38207600-38224000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:38208000-38220600	Weak transcription	NH-A	brain
5	chr13:38208200-38219200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr13:38209400-38219000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr13:38209400-38219200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:38210000-38219600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:38211400-38221200	Weak transcription	NHDF-Ad	bronchial
10	chr13:38211400-38275600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr13:38211600-38221200	Weak transcription	Ovary	ovary
12	chr13:38212400-38219200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr13:38213000-38219200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr13:38214400-38215400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr13:38214400-38215600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr13:38214400-38216200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:38214600-38216000	Enhancers	Osteobl	bone

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