Variant report

Variant	rs432981
Chromosome Location	chr2:40434262-40434263
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs1641452	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1641456	0.83[ASN][1000 genomes]
rs1641457	0.83[ASN][1000 genomes]
rs1641458	0.83[ASN][1000 genomes]
rs1651355	0.83[ASN][1000 genomes]
rs1651356	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34971853	0.83[ASN][1000 genomes]
rs36162999	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36184451	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs368642	0.84[ASN][1000 genomes]
rs369140	0.83[ASN][1000 genomes]
rs371909	0.91[ASN][1000 genomes]
rs372052	0.83[ASN][1000 genomes]
rs374159	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs374711	0.84[ASN][1000 genomes]
rs375180	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs376170	0.83[ASN][1000 genomes]
rs376491	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs379410	0.84[ASN][1000 genomes]
rs379859	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs380975	0.83[ASN][1000 genomes]
rs383073	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs384511	0.81[ASN][1000 genomes]
rs384791	0.83[ASN][1000 genomes]
rs384994	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs385561	0.83[ASN][1000 genomes]
rs389109	0.83[ASN][1000 genomes]
rs389992	0.86[ASN][1000 genomes]
rs391984	0.85[ASN][1000 genomes]
rs393711	0.83[ASN][1000 genomes]
rs399061	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs401815	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs402307	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs406736	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs407267	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs408662	0.84[ASN][1000 genomes]
rs410480	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs413711	0.81[ASN][1000 genomes]
rs415695	0.81[ASN][1000 genomes]
rs417464	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs417873	0.84[ASN][1000 genomes]
rs418380	0.83[ASN][1000 genomes]
rs422411	0.81[ASN][1000 genomes]
rs423075	0.84[ASN][1000 genomes]
rs426295	0.83[ASN][1000 genomes]
rs427632	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs428738	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs429227	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs430314	0.81[ASN][1000 genomes]
rs430394	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs430473	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs432142	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs432769	0.85[ASN][1000 genomes]
rs434326	0.83[ASN][1000 genomes]
rs436010	0.86[ASN][1000 genomes]
rs439960	0.84[ASN][1000 genomes]
rs441802	0.85[ASN][1000 genomes]
rs442476	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs442586	0.91[ASN][1000 genomes]
rs443236	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs444504	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs450116	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs450823	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs452138	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs479909	0.97[ASN][1000 genomes]
rs4952596	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs581477	0.81[ASN][1000 genomes]
rs581568	0.81[ASN][1000 genomes]
rs588179	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs615449	0.91[ASN][1000 genomes]
rs666362	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs678107	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs679339	0.84[ASN][1000 genomes]
rs72794789	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv873902	chr2:40231282-40466268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1004092	chr2:40264608-40451701	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1000572	chr2:40271958-40458911	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv535654	chr2:40271958-40458911	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv581502	chr2:40273903-40459645	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv873904	chr2:40292289-40466268	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv873910	chr2:40391907-40466268	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	esv1851152	chr2:40393223-40512023	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv526425	chr2:40418386-40447587	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv526074	chr2:40423454-40451724	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv873911	chr2:40423454-41161464	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv1008190	chr2:40429442-40506772	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:40418200-40447200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr2:40418600-40445800	Weak transcription	Dnd41	blood
3	chr2:40419200-40436600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:40422000-40435200	Weak transcription	Fetal Kidney	kidney
5	chr2:40422600-40436400	Weak transcription	Right Ventricle	heart
6	chr2:40430600-40439600	Weak transcription	HSMM	muscle
7	chr2:40430800-40435000	Weak transcription	Osteobl	bone
8	chr2:40430800-40439800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:40431200-40436400	Weak transcription	Left Ventricle	heart
10	chr2:40431200-40440600	Weak transcription	Fetal Stomach	stomach
11	chr2:40431400-40439800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:40431400-40440200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:40431600-40434800	Weak transcription	Fetal Heart	heart
14	chr2:40431600-40436400	Weak transcription	Colon Smooth Muscle	Colon
15	chr2:40431800-40434600	Weak transcription	Fetal Brain Male	brain
16	chr2:40431800-40435000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:40431800-40440000	Weak transcription	NHDF-Ad	bronchial
18	chr2:40432200-40440200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:40433400-40434600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:40434000-40435000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:40434200-40437200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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