Variant report

Variant	rs6710361
Chromosome Location	chr2:87047145-87047146
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12994456	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13019439	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13023213	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13024420	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13024609	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13032379	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1515950	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3020726	1.00[ASN][1000 genomes]
rs3020728	0.87[ASN][1000 genomes]
rs34198915	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34256565	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34492196	1.00[ASN][1000 genomes]
rs34546581	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34613828	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34813683	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34855635	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34988194	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35290870	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35437846	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35505884	0.97[ASN][1000 genomes]
rs35626322	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35723887	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35739120	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35786939	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3810831	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4366909	1.00[ASN][1000 genomes]
rs4832315	0.85[ASN][1000 genomes]
rs55816457	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55817008	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6755452	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71411867	1.00[ASN][1000 genomes]
rs71411868	0.90[EUR][1000 genomes]
rs71411869	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7596329	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532724	chr2:86622295-87086407	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv10063	chr2:86940988-87084360	Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1002420	chr2:86948835-87172715	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv874472	chr2:86961252-87071474	Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv1008817	chr2:86970406-87172715	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	esv14382	chr2:86972214-87174121	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv997982	chr2:86972834-87105864	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv1007746	chr2:86972834-87172715	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv458585	chr2:86974318-87108211	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
10	nsv582373	chr2:86974318-87108211	Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv1007307	chr2:86974563-87055214	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
12	nsv535809	chr2:86974563-87055214	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv1004572	chr2:86975514-87082883	Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv535811	chr2:86975514-87082883	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
15	nsv532319	chr2:87024867-88005418	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
16	nsv961427	chr2:87032925-87059989	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 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	chr2:87035600-87048800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:87037200-87048000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:87037200-87048800	Weak transcription	Esophagus	oesophagus
4	chr2:87041000-87048600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:87045000-87048400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr2:87045600-87047600	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr2:87045600-87048600	Enhancers	Primary T cells from cord blood	blood
8	chr2:87045800-87048600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr2:87046000-87048000	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr2:87046200-87048000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr2:87046600-87047400	Enhancers	Thymus	Thymus
12	chr2:87046800-87051000	Genic enhancers	Fetal Thymus	thymus
13	chr2:87047000-87049000	Weak transcription	Dnd41	blood

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