Variant report

Variant	rs10251218
Chromosome Location	chr7:110711714-110711715
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10230261	1.00[YRI][hapmap]
rs10232461	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10232632	1.00[YRI][hapmap]
rs10232638	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10234323	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10235471	1.00[AMR][1000 genomes]
rs10239308	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10239982	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10242243	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10242510	1.00[AFR][1000 genomes]
rs10247851	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10248799	1.00[YRI][hapmap]
rs10253600	1.00[YRI][hapmap]
rs10257658	1.00[AFR][1000 genomes]
rs10260023	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10260878	1.00[YRI][hapmap]
rs10261952	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10262121	1.00[YRI][hapmap]
rs10263280	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10266618	1.00[AMR][1000 genomes]
rs10266806	1.00[AMR][1000 genomes]
rs10266977	1.00[YRI][hapmap]
rs10267717	1.00[YRI][hapmap]
rs10276462	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10278436	1.00[AMR][1000 genomes]
rs10279604	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10282078	1.00[YRI][hapmap]
rs13438044	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13438736	1.00[YRI][hapmap]
rs28401368	1.00[AFR][1000 genomes]
rs28415597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28520723	1.00[AFR][1000 genomes]
rs28524030	1.00[AFR][1000 genomes]
rs28533798	1.00[AFR][1000 genomes]
rs28535164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28568792	1.00[AFR][1000 genomes]
rs28729497	1.00[AFR][1000 genomes]
rs28890022	0.89[AFR][1000 genomes]
rs6949309	1.00[YRI][hapmap]
rs6968936	1.00[AMR][1000 genomes]
rs7810421	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531434	chr7:110310931-110839892	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3506497	chr7:110484691-111091738	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3506498	chr7:110484750-111091689	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2758129	chr7:110523298-110787849	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759554	chr7:110523298-110787849	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1031546	chr7:110549137-110978256	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv817555	chr7:110564801-110990927	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1033286	chr7:110588021-110990928	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv539063	chr7:110588021-110990928	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv931978	chr7:110607590-111092490	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv1025987	chr7:110609568-111258501	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	esv2830178	chr7:110645431-110778571	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1024477	chr7:110660006-110944477	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv608154	chr7:110688993-110945501	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110690800-110714400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:110705600-110714000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:110707000-110714800	Enhancers	Primary T cells from cord blood	blood
4	chr7:110707400-110711800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr7:110707600-110717800	Weak transcription	Right Atrium	heart
6	chr7:110710600-110712600	Weak transcription	Adipose Nuclei	Adipose
7	chr7:110711200-110712200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr7:110711200-110715000	Enhancers	Dnd41	blood
9	chr7:110711600-110711800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr7:110711600-110711800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr7:110711600-110712000	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:110711600-110712400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr7:110711600-110712600	Enhancers	Primary T helper cells fromperipheralblood	blood

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