Variant report

Variant	rs59441022
Chromosome Location	chr4:8702667-8702668
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	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10001200	0.83[EUR][1000 genomes]
rs10011857	0.90[EUR][1000 genomes]
rs10938736	0.96[EUR][1000 genomes]
rs10938737	0.91[EUR][1000 genomes]
rs10938738	0.86[EUR][1000 genomes]
rs10938739	0.86[EUR][1000 genomes]
rs11726615	0.91[EUR][1000 genomes]
rs11727668	0.90[EUR][1000 genomes]
rs11732207	0.86[EUR][1000 genomes]
rs12647939	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12647943	0.91[EUR][1000 genomes]
rs13105029	0.86[EUR][1000 genomes]
rs13122836	0.84[EUR][1000 genomes]
rs13122842	0.84[EUR][1000 genomes]
rs28626694	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28706964	0.81[EUR][1000 genomes]
rs4076895	0.91[EUR][1000 genomes]
rs4077319	0.96[EUR][1000 genomes]
rs4078060	0.83[EUR][1000 genomes]
rs4522850	0.83[EUR][1000 genomes]
rs4696718	0.85[EUR][1000 genomes]
rs4696719	0.86[EUR][1000 genomes]
rs4696911	0.83[EUR][1000 genomes]
rs4696917	0.91[EUR][1000 genomes]
rs56223652	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58124893	0.84[EUR][1000 genomes]
rs58405044	0.81[EUR][1000 genomes]
rs6447889	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6447890	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6447891	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6447892	0.96[EUR][1000 genomes]
rs6447893	0.96[EUR][1000 genomes]
rs6813673	0.90[EUR][1000 genomes]
rs6843081	0.82[EUR][1000 genomes]
rs6850363	0.96[EUR][1000 genomes]
rs73802722	0.84[EUR][1000 genomes]
rs7434700	0.86[EUR][1000 genomes]
rs7435116	0.91[EUR][1000 genomes]
rs7438091	0.86[EUR][1000 genomes]
rs7438203	0.91[EUR][1000 genomes]
rs7438715	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7440872	0.91[EUR][1000 genomes]
rs7442075	0.83[EUR][1000 genomes]
rs7657647	0.96[EUR][1000 genomes]
rs7663016	0.96[EUR][1000 genomes]
rs7663720	0.91[EUR][1000 genomes]
rs7665898	0.83[EUR][1000 genomes]
rs7679132	0.89[EUR][1000 genomes]
rs7682634	0.96[EUR][1000 genomes]
rs7683992	0.83[EUR][1000 genomes]
rs7686852	0.99[EUR][1000 genomes]
rs7698224	0.83[EUR][1000 genomes]
rs7698226	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
2	esv1832730	chr4:8541086-9514568	Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	esv1843578	chr4:8541086-9514568	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv878617	chr4:8566758-9371116	ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv1014219	chr4:8578779-8724531	Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv470015	chr4:8584879-8729638	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv878621	chr4:8584879-9371116	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
8	nsv878622	chr4:8599250-9371116	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
9	nsv829855	chr4:8604879-8729607	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv915590	chr4:8607839-9558139	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
11	esv1792139	chr4:8619465-9407085	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
12	esv1821058	chr4:8621252-9370511	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
13	esv1792999	chr4:8622394-9370511	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
14	esv1819636	chr4:8622394-9370511	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
15	esv1829855	chr4:8622394-9370511	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
16	esv1845492	chr4:8622394-9370511	Enhancers Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
17	nsv461222	chr4:8644223-8729638	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
18	nsv593642	chr4:8644223-8729638	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv878623	chr4:8644223-9371116	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
20	nsv878624	chr4:8656976-9371116	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
21	nsv878625	chr4:8683744-9371116	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
22	nsv593645	chr4:8694389-8729471	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	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	chr4:8701600-8703400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:8702000-8702800	Bivalent Enhancer	Fetal Stomach	stomach
3	chr4:8702000-8703000	Bivalent Enhancer	Fetal Lung	lung
4	chr4:8702200-8703600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:8702400-8702800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
6	chr4:8702400-8702800	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:8702600-8702800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:8702600-8702800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:8702600-8702800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:8702600-8703000	Bivalent Enhancer	Stomach Smooth Muscle	stomach

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