Variant report

Variant	rs7574649
Chromosome Location	chr2:101102943-101102944
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:101101769..101103821-chr2:101257032..101259375,2	K562	blood:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs12614705	1.00[CEU][hapmap]
rs12619028	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12619423	0.91[EUR][1000 genomes]
rs12620497	0.91[EUR][1000 genomes]
rs12620836	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12621241	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12623984	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17024288	1.00[EUR][1000 genomes]
rs17024415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17024421	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17024434	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17024457	1.00[CEU][hapmap]
rs17024467	0.91[EUR][1000 genomes]
rs17024471	0.91[EUR][1000 genomes]
rs17024473	0.91[EUR][1000 genomes]
rs17024480	0.91[EUR][1000 genomes]
rs17354256	1.00[AFR][1000 genomes]
rs55796343	1.00[EUR][1000 genomes]
rs55827030	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55849205	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56100007	0.91[EUR][1000 genomes]
rs61620481	0.91[EUR][1000 genomes]
rs61647034	0.91[EUR][1000 genomes]
rs6705910	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6709376	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6709957	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6730520	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6738492	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6745149	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72821202	1.00[EUR][1000 genomes]
rs72823210	1.00[EUR][1000 genomes]
rs72823211	1.00[EUR][1000 genomes]
rs72823212	1.00[EUR][1000 genomes]
rs72823215	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72823243	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72823244	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72823245	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72823252	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72823264	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72823265	0.91[EUR][1000 genomes]
rs72823266	0.91[EUR][1000 genomes]
rs72823268	0.91[EUR][1000 genomes]
rs72823269	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72823271	0.91[EUR][1000 genomes]
rs72823274	0.91[EUR][1000 genomes]
rs72823277	0.91[EUR][1000 genomes]
rs72825294	0.91[EUR][1000 genomes]
rs72825295	0.91[EUR][1000 genomes]
rs72825302	1.00[EUR][1000 genomes]
rs7577785	1.00[EUR][1000 genomes]
rs7587950	0.91[EUR][1000 genomes]
rs7597493	1.00[CEU][hapmap]
rs7604140	1.00[EUR][1000 genomes]
rs7604590	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7608774	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007777	chr2:100816913-101308914	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv535844	chr2:100816913-101308914	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv582531	chr2:100908508-101207639	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv916792	chr2:101021066-101525200	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv582532	chr2:101029002-101531943	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv1011990	chr2:101039956-101105648	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv834312	chr2:101044438-101238166	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv582533	chr2:101086151-101103384	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:101095600-101104200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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