Variant report

Variant	rs13010262
Chromosome Location	chr2:145781546-145781547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10496971	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11689317	0.88[AMR][1000 genomes]
rs12616953	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12621647	0.86[AMR][1000 genomes]
rs12990953	0.84[ASN][1000 genomes]
rs13001583	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13004410	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13009916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010313	0.86[AMR][1000 genomes]
rs13033869	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1371047	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16824386	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1898732	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1918876	0.80[GIH][hapmap]
rs2381685	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs34409381	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34948552	0.86[AMR][1000 genomes]
rs34985138	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4662413	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56014517	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56795645	0.83[AMR][1000 genomes]
rs67431032	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs67969609	0.92[AMR][1000 genomes];0.84[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	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv932113	chr2:145515124-145844491	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv834398	chr2:145659419-145830156	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv431768	chr2:145741527-145981491	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145771200-145782600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:145780000-145783000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:145780400-145782000	Active TSS	NHLF	lung
4	chr2:145780400-145783000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:145780400-145784200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:145780600-145787400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:145780800-145784200	Weak transcription	Fetal Lung	lung
8	chr2:145781000-145781600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr2:145781000-145781800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:145781000-145781800	Flanking Active TSS	Osteobl	bone
11	chr2:145781000-145782000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:145781000-145784200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr2:145781000-145785600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:145781200-145781800	Flanking Active TSS	A549	lung
15	chr2:145781200-145782000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:145781200-145785800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:145781400-145781600	Active TSS	NHDF-Ad	bronchial
18	chr2:145781400-145784200	Weak transcription	Ovary	ovary
19	chr2:145781400-145784200	Weak transcription	HSMMtube	muscle
20	chr2:145781400-145785000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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