Variant report

Variant	rs61119489
Chromosome Location	chr4:75138666-75138667
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:75138132..75141011-chr4:75168302..75170057,2	K562	blood:
2	chr4:75138324..75140487-chr4:75143811..75148058,4	K562	blood:
3	chr4:75131662..75133777-chr4:75138644..75141998,3	K562	blood:

Variant related genes	Relation type
ENSG00000163738	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1460005	1.00[EUR][1000 genomes]
rs16850793	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16850798	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16850813	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16850818	1.00[EUR][1000 genomes]
rs16850842	1.00[EUR][1000 genomes]
rs16850845	1.00[EUR][1000 genomes]
rs16850847	1.00[EUR][1000 genomes]
rs16850852	1.00[EUR][1000 genomes]
rs16850933	1.00[EUR][1000 genomes]
rs16850945	1.00[EUR][1000 genomes]
rs1993664	1.00[EUR][1000 genomes]
rs56192801	1.00[EUR][1000 genomes]
rs57516973	1.00[EUR][1000 genomes]
rs58215609	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58398242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59142088	1.00[EUR][1000 genomes]
rs59172186	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59175703	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60181583	1.00[EUR][1000 genomes]
rs60560556	1.00[EUR][1000 genomes]
rs6830535	1.00[EUR][1000 genomes]
rs6836879	1.00[EUR][1000 genomes]
rs725142	1.00[EUR][1000 genomes]
rs73824433	1.00[EUR][1000 genomes]
rs73824435	1.00[EUR][1000 genomes]
rs73824446	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73824447	1.00[EUR][1000 genomes]
rs73824448	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73824449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73824453	1.00[EUR][1000 genomes]
rs73824457	1.00[EUR][1000 genomes]
rs73824458	1.00[EUR][1000 genomes]
rs73824469	1.00[EUR][1000 genomes]
rs922136	1.00[EUR][1000 genomes]
rs9685225	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1009099	chr4:75089233-75726206	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75119800-75148800	Weak transcription	Aorta	Aorta
2	chr4:75120000-75141200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:75125200-75142600	Weak transcription	K562	blood
4	chr4:75125200-75158800	Weak transcription	Left Ventricle	heart
5	chr4:75130000-75140200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:75132200-75157800	Weak transcription	Brain Hippocampus Middle	brain
7	chr4:75133800-75160000	Weak transcription	Liver	Liver
8	chr4:75134000-75173800	Weak transcription	Primary T cells from cord blood	blood
9	chr4:75134400-75148800	Weak transcription	HSMM	muscle
10	chr4:75134600-75148400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:75134800-75148200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:75134800-75148200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:75134800-75148800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:75135000-75147600	Weak transcription	HMEC	breast
15	chr4:75135600-75143000	Weak transcription	NHEK	skin
16	chr4:75138000-75140200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:75138400-75139200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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