Variant report

Variant	rs2037799
Chromosome Location	chr2:182625313-182625314
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:182622819..182625911-chr2:182627931..182631069,3	K562	blood:
2	chr2:182621687..182624059-chr2:182624829..182627289,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10165936	0.96[YRI][hapmap];0.82[AFR][1000 genomes]
rs10173114	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs10179363	0.89[YRI][hapmap]
rs10179547	0.82[ASW][hapmap];0.83[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10183527	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10183937	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs10190772	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10803953	0.92[CHB][hapmap];0.89[ASN][1000 genomes]
rs10930979	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11884097	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11886921	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11895376	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11901603	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11902910	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13414894	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13415272	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13419200	1.00[TSI][hapmap]
rs13424337	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13425734	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs13428496	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1343793	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16867494	0.81[CHB][hapmap]
rs16867495	0.85[JPT][hapmap]
rs16867502	0.86[CHD][hapmap]
rs1881159	0.86[YRI][hapmap]
rs2368225	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2582999	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4018749	0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs57930770	0.87[ASN][1000 genomes]
rs60384758	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6730859	0.83[AFR][1000 genomes]
rs6740944	0.87[ASN][1000 genomes]
rs6748354	0.93[YRI][hapmap]
rs6754481	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7567220	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7567371	0.87[ASN][1000 genomes]
rs7595805	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9288073	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9288074	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs937296	0.81[ASN][1000 genomes]
rs951542	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs951543	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1001558	chr2:182590009-182732738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182616800-182631000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:182619800-182629000	Weak transcription	Stomach Mucosa	stomach
3	chr2:182624800-182627000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:182625000-182625400	Enhancers	Fetal Kidney	kidney
5	chr2:182625000-182625600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:182625000-182625800	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:182625000-182627000	Enhancers	Brain Hippocampus Middle	brain
8	chr2:182625200-182626000	Enhancers	Primary hematopoietic stem cells	blood
9	chr2:182625200-182626000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:182625200-182626200	Weak transcription	Brain Substantia Nigra	brain
11	chr2:182625200-182629800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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