Variant report

Variant	rs17440818
Chromosome Location	chr5:107365091-107365092
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:107364061..107366146-chr5:107369915..107372470,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10037490	0.87[EUR][1000 genomes]
rs10056741	0.80[EUR][1000 genomes]
rs10077316	0.80[EUR][1000 genomes]
rs10440792	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10515384	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12651724	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12651919	0.81[CEU][hapmap];0.86[EUR][1000 genomes]
rs12652306	0.81[EUR][1000 genomes]
rs12652643	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12652687	1.00[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];0.88[EUR][1000 genomes]
rs12652883	0.88[EUR][1000 genomes]
rs12654751	1.00[CEU][hapmap];0.87[CHB][hapmap];0.93[JPT][hapmap];0.90[EUR][1000 genomes]
rs12655475	0.88[EUR][1000 genomes]
rs12655573	0.87[EUR][1000 genomes]
rs12655932	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12656140	0.87[EUR][1000 genomes]
rs12659666	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13357987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17160869	0.82[YRI][hapmap]
rs17381296	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17382278	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17383035	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17384285	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.83[EUR][1000 genomes]
rs17437658	0.87[EUR][1000 genomes]
rs17438307	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs17439150	0.90[EUR][1000 genomes]
rs17439877	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17440508	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17440916	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17441920	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17442211	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17442556	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap]
rs17442864	0.89[JPT][hapmap];0.88[EUR][1000 genomes]
rs17443045	0.87[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes]
rs17449654	1.00[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap];0.84[EUR][1000 genomes]
rs17449723	1.00[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap];0.84[EUR][1000 genomes]
rs2042187	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28670811	0.87[EUR][1000 genomes]
rs286751	0.80[CHB][hapmap]
rs289232	0.87[CHB][hapmap]
rs4144476	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4144478	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4404664	0.88[EUR][1000 genomes]
rs4582260	0.87[EUR][1000 genomes]
rs55780614	0.88[EUR][1000 genomes]
rs55862455	0.88[EUR][1000 genomes]
rs55958078	0.82[EUR][1000 genomes]
rs56108486	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56287990	0.84[EUR][1000 genomes]
rs58342334	0.88[EUR][1000 genomes]
rs58805667	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59356989	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59606487	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59711822	0.88[EUR][1000 genomes]
rs59830006	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60447697	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6596766	0.82[EUR][1000 genomes]
rs6864731	0.90[EUR][1000 genomes]
rs6865057	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6872068	0.88[EUR][1000 genomes]
rs6872913	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6884026	0.88[EUR][1000 genomes]
rs6889772	0.88[EUR][1000 genomes]
rs6890052	0.87[EUR][1000 genomes]
rs723397	0.93[CEU][hapmap];0.86[CHB][hapmap];0.95[EUR][1000 genomes]
rs73204759	0.87[EUR][1000 genomes]
rs73204760	0.87[EUR][1000 genomes]
rs73204762	0.84[EUR][1000 genomes]
rs73204763	0.87[EUR][1000 genomes]
rs73204764	0.87[EUR][1000 genomes]
rs73204766	0.87[EUR][1000 genomes]
rs73204790	0.88[EUR][1000 genomes]
rs73204796	0.90[EUR][1000 genomes]
rs73206507	0.89[EUR][1000 genomes]
rs73206538	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7704251	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7731562	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7735773	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882682	chr5:107213361-107458336	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv534281	chr5:107357579-107674981	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3435266	chr5:107362345-107373452	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3469699	chr5:107362374-107373448	Weak transcription Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3469701	chr5:107362374-107373448	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3469700	chr5:107362376-107373479	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107339600-107373800	Weak transcription	Primary T cells from cord blood	blood
2	chr5:107361000-107369800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:107361200-107368000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:107361600-107369200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:107363800-107365200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:107364000-107365200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr5:107364000-107365200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:107364000-107390000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr5:107364200-107365200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:107364200-107365200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:107364400-107373200	Weak transcription	Pancreas	Pancrea

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