Variant report

Variant	rs7583318
Chromosome Location	chr2:38856983-38856984
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:38853457..38857426-chr2:38859030..38862948,5	K562	blood:
2	chr2:38856981..38859644-chr2:38870744..38873095,2	K562	blood:
3	chr2:38850084..38852366-chr2:38855789..38858760,2	K562	blood:
4	chr2:38826731..38830931-chr2:38855127..38860520,4	MCF-7	breast:
5	chr2:38850355..38852366-chr2:38854447..38858679,3	K562	blood:

Variant related genes	Relation type
ENSG00000235586	Chromatin interaction
ENSG00000143889	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10204680	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12992482	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13010091	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13011896	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13015860	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13016108	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13016885	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13025153	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13415823	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13432435	0.83[EUR][1000 genomes]
rs13432610	0.83[AMR][1000 genomes]
rs17022983	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17493692	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17575960	0.81[ASN][1000 genomes]
rs2116383	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2116385	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2163551	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2217537	0.85[EUR][1000 genomes]
rs2373420	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2373422	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34145681	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34450185	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35273515	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35613649	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35861429	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67326552	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6742843	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6745646	0.85[EUR][1000 genomes]
rs6749343	0.85[ASN][1000 genomes]
rs72909831	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7561778	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7600802	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs919698	0.81[ASN][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	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv873881	chr2:38745624-38877636	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv581482	chr2:38799820-38858669	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv581483	chr2:38799820-38862223	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv581484	chr2:38799820-38874177	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv581485	chr2:38839323-38893660	Weak transcription Enhancers Flanking Active TSS Active TSS 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	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38835400-38862400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:38854000-38861200	Weak transcription	Primary T cells from cord blood	blood
3	chr2:38855600-38857000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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