Variant report

Variant	rs72611197
Chromosome Location	chr4:598025-598026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:596162..597825-chr4:597849..599357,2	MCF-7	breast:
2	chr4:594354..601823-chr4:659072..674169,20	MCF-7	breast:
3	chr4:595977..599927-chr4:674651..678190,4	MCF-7	breast:
4	chr4:595274..598065-chr4:602440..604215,2	K562	blood:

Variant related genes	Relation type
ENSG00000169020	Chromatin interaction
ENSG00000215375	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10007206	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10007497	0.93[ASN][1000 genomes]
rs10011154	0.91[ASN][1000 genomes]
rs10023472	0.87[ASN][1000 genomes]
rs10027866	0.87[ASN][1000 genomes]
rs10029928	0.93[ASN][1000 genomes]
rs10031745	0.92[ASN][1000 genomes]
rs10031968	0.93[ASN][1000 genomes]
rs11248029	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13107358	0.95[ASN][1000 genomes]
rs28374488	0.88[ASN][1000 genomes]
rs28380593	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28403281	0.99[ASN][1000 genomes]
rs28438498	0.86[ASN][1000 genomes]
rs28476575	0.93[ASN][1000 genomes]
rs28504161	0.91[ASN][1000 genomes]
rs28588872	0.87[ASN][1000 genomes]
rs28600205	0.86[ASN][1000 genomes]
rs28714509	0.99[ASN][1000 genomes]
rs28754797	0.93[ASN][1000 genomes]
rs28769407	0.99[ASN][1000 genomes]
rs28826275	0.99[ASN][1000 genomes]
rs34307246	0.99[ASN][1000 genomes]
rs3888807	0.91[ASN][1000 genomes]
rs4075653	0.93[ASN][1000 genomes]
rs59623849	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67030464	0.86[ASN][1000 genomes]
rs67376373	0.81[ASN][1000 genomes]
rs67703486	0.93[ASN][1000 genomes]
rs72611195	0.92[ASN][1000 genomes]
rs72611198	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72611199	0.99[ASN][1000 genomes]
rs72611200	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72611201	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72611202	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72613103	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72613104	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72613105	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72613106	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72613107	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72613108	0.87[ASN][1000 genomes]
rs7438471	0.93[ASN][1000 genomes]
rs7661376	0.99[ASN][1000 genomes]
rs7669178	0.89[EUR][1000 genomes]
rs9884240	0.99[ASN][1000 genomes]
rs9997286	0.93[ASN][1000 genomes]
rs9998967	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv532703	chr4:72447-614414	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv532704	chr4:85040-628550	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
8	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
11	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs72611197	RP11-1191J2.2	cis	Skin Sun Exposed Lower leg	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:593600-605800	Weak transcription	Right Atrium	heart
2	chr4:594800-604200	Weak transcription	Brain Anterior Caudate	brain
3	chr4:596600-598600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr4:596600-598800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:596600-599000	Enhancers	Primary hematopoietic stem cells	blood
6	chr4:596800-598600	Enhancers	Primary T cells from cord blood	blood
7	chr4:597000-598400	Weak transcription	Fetal Thymus	thymus
8	chr4:597600-598800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:597800-598200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:597800-598600	Enhancers	Dnd41	blood
11	chr4:598000-598200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr4:598000-598400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:598000-598600	Enhancers	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links