Variant report

Variant	rs2024843
Chromosome Location	chr6:101460679-101460680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs11755579	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs11758174	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs11759127	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs13205402	0.91[ASN][1000 genomes]
rs13212730	0.91[ASN][1000 genomes]
rs13220881	0.89[ASN][1000 genomes]
rs1337385	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1406894	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17801075	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1813223	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs1923013	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2004276	0.87[ASN][1000 genomes]
rs2024842	0.84[ASN][1000 genomes]
rs2398247	0.86[ASN][1000 genomes]
rs34555727	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4240589	0.99[ASN][1000 genomes]
rs4464803	0.93[ASN][1000 genomes]
rs4840157	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs4840160	0.89[ASN][1000 genomes]
rs4840164	0.91[ASN][1000 genomes]
rs4840169	0.84[ASN][1000 genomes]
rs4840170	0.84[ASN][1000 genomes]
rs55967215	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56359216	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588204	0.91[ASN][1000 genomes]
rs599934	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs62419249	0.84[ASN][1000 genomes]
rs62420689	0.89[ASN][1000 genomes]
rs62420692	0.96[ASN][1000 genomes]
rs652335	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs669543	0.90[ASN][1000 genomes]
rs679444	0.86[ASN][1000 genomes]
rs684140	0.95[ASN][1000 genomes]
rs694418	0.90[ASN][1000 genomes]
rs7453078	0.94[ASN][1000 genomes]
rs7740902	0.81[EUR][1000 genomes]
rs7758630	0.91[ASN][1000 genomes]
rs7760958	0.92[EUR][1000 genomes]
rs7769142	0.84[ASN][1000 genomes]
rs7772462	0.99[ASN][1000 genomes]
rs9322270	0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9322271	0.87[ASN][1000 genomes]
rs9322276	0.86[ASN][1000 genomes]
rs9377241	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs9377251	0.99[ASN][1000 genomes]
rs9390698	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs9404060	0.87[ASN][1000 genomes]
rs9404069	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9404070	0.92[EUR][1000 genomes]
rs979122	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs9791225	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101459000-101461400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr6:101459400-101461400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:101459600-101460800	Enhancers	Primary T cells from cord blood	blood
4	chr6:101459600-101460800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr6:101459600-101461200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:101459800-101461200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr6:101459800-101461400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:101459800-101461800	Enhancers	Dnd41	blood
9	chr6:101459800-101462400	Weak transcription	Liver	Liver
10	chr6:101459800-101463200	Weak transcription	Fetal Intestine Small	intestine

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