Variant report

Variant	rs17204072
Chromosome Location	chr4:91008877-91008878
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	chr4:91007942..91012352-chr4:91047330..91049879,3	MCF-7	breast:
2	chr4:91008351..91011205-chr4:91046024..91048937,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184305	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10516857	0.81[EUR][1000 genomes]
rs10516858	0.92[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10516860	0.82[EUR][1000 genomes]
rs10516862	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10516864	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11732065	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12500465	0.81[EUR][1000 genomes]
rs12639636	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12642395	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12642404	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12647171	0.83[EUR][1000 genomes]
rs12647266	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12648872	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12649987	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12650363	0.83[EUR][1000 genomes]
rs12651123	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13103611	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13104940	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13107286	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13108338	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13113863	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13119778	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13120745	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13121853	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13124133	0.82[EUR][1000 genomes]
rs13131070	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13131903	0.80[EUR][1000 genomes]
rs13132515	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13132730	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13148977	0.81[EUR][1000 genomes]
rs13149395	0.87[EUR][1000 genomes]
rs13150124	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13151441	0.82[EUR][1000 genomes]
rs1443796	0.82[EUR][1000 genomes]
rs1562034	0.82[EUR][1000 genomes]
rs17204198	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17205805	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17808648	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17808829	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs1812076	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1835521	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1982293	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2120372	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2120375	0.80[EUR][1000 genomes]
rs34001515	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34064092	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34146382	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34243515	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34343229	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34886505	0.86[EUR][1000 genomes]
rs35197902	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36047807	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55663876	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55686873	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62312738	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62312743	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62313888	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62313890	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6532212	0.81[EUR][1000 genomes]
rs6814978	0.82[EUR][1000 genomes]
rs6819755	0.82[EUR][1000 genomes]
rs6830014	0.83[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6837222	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs723992	0.81[EUR][1000 genomes]
rs72659470	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7438673	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7660182	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7661577	0.81[EUR][1000 genomes]
rs7672024	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7677884	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7677966	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7685355	0.81[EUR][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	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv879537	chr4:90883047-91165346	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv830006	chr4:90971656-91186340	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv879538	chr4:90993172-91080308	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 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	chr4:91008800-91009200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links