Variant report

Variant	rs7309785
Chromosome Location	chr12:10610546-10610547
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	YY1	chr12:10610285-10610837	H1-hESC	embryonic stem cell:	n/a	chr12:10610458-10610470 chr12:10610500-10610512
2	YY1	chr12:10610255-10610701	H1-hESC	embryonic stem cell:	n/a	chr12:10610458-10610470 chr12:10610500-10610512
3	TAF1	chr12:10610276-10610758	H1-hESC	embryonic stem cell:	n/a	n/a
4	POU5F1	chr12:10610279-10610703	H1-hESC	embryonic stem cell:	n/a	n/a
5	MAX	chr12:10610385-10610592	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
KLRC1	TF binding region

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10845143	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11053808	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11830819	0.87[EUR][1000 genomes]
rs12424871	0.80[ASN][1000 genomes]
rs12426187	0.82[ASN][1000 genomes]
rs12427017	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs12814304	0.87[EUR][1000 genomes]
rs12819494	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12821887	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12824469	0.87[EUR][1000 genomes]
rs12826560	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12830618	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1851072	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1971939	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs2253365	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs2294148	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs2417740	0.85[EUR][1000 genomes]
rs2417741	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2417897	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2417898	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35078927	0.87[EUR][1000 genomes]
rs35318826	0.88[EUR][1000 genomes]
rs35683234	0.87[EUR][1000 genomes]
rs3809215	0.82[ASN][1000 genomes]
rs3809216	0.82[ASN][1000 genomes]
rs57106039	0.84[ASN][1000 genomes]
rs59372234	0.84[ASN][1000 genomes]
rs60018231	0.84[ASN][1000 genomes]
rs60078099	0.80[ASN][1000 genomes]
rs60248367	0.84[ASN][1000 genomes]
rs61571638	0.82[ASN][1000 genomes]
rs6488287	0.84[ASN][1000 genomes]
rs6488296	0.84[EUR][1000 genomes]
rs7134846	0.83[ASN][1000 genomes]
rs7135238	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7138294	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72475450	0.80[ASN][1000 genomes]
rs72475451	0.80[ASN][1000 genomes]
rs72475452	0.80[ASN][1000 genomes]
rs728010	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7303771	0.84[EUR][1000 genomes]
rs7310149	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7342353	0.87[EUR][1000 genomes]
rs74062025	0.82[ASN][1000 genomes]
rs74062026	0.82[ASN][1000 genomes]
rs7952993	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs7953443	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs7955196	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7962112	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7969985	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs7972757	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7980470	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832328	chr12:10398071-10620443	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv8914	chr12:10532300-10662676	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv557456	chr12:10532326-10698255	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv898764	chr12:10537269-10698255	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv898765	chr12:10537269-10701992	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv898766	chr12:10537269-10722585	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
8	nsv557457	chr12:10545925-10698255	Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv557458	chr12:10546140-10698255	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv606	chr12:10552632-10612899	Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv898767	chr12:10553930-10622047	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv557459	chr12:10560591-10729821	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv870117	chr12:10565955-10648821	Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv557477	chr12:10601690-10698255	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv557478	chr12:10604945-10698255	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 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	chr12:10607600-10625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:10609600-10611000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr12:10609600-10611000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr12:10610000-10610800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:10610000-10610800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:10610000-10611000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr12:10610200-10610800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr12:10610400-10610600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:10610400-10610800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:10610400-10610800	Active TSS	iPS-20b Cell Line	embryonic stem cell

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