Variant report

Variant	rs61181974
Chromosome Location	chr6:163618155-163618156
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10214583	1.00[EUR][1000 genomes]
rs56216041	1.00[EUR][1000 genomes]
rs58829423	1.00[EUR][1000 genomes]
rs58858933	1.00[EUR][1000 genomes]
rs60020523	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61170720	1.00[AFR][1000 genomes]
rs6901770	1.00[EUR][1000 genomes]
rs6903043	1.00[EUR][1000 genomes]
rs6915979	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929615	1.00[EUR][1000 genomes]
rs73784512	1.00[EUR][1000 genomes]
rs7742100	1.00[EUR][1000 genomes]
rs7766922	1.00[EUR][1000 genomes]
rs7768185	1.00[EUR][1000 genomes]
rs9295210	1.00[EUR][1000 genomes]
rs9456836	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1026490	chr6:163133433-163705708	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer 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	8 gene(s)	inside rSNPs	diseases
3	nsv869286	chr6:163146342-163697445	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2762628	chr6:163572148-163620903	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr6:163602600-163622600	Weak transcription	Right Ventricle	heart
2	chr6:163608000-163632800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:163614000-163621200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:163614200-163618800	Weak transcription	Fetal Heart	heart
5	chr6:163616400-163628800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr6:163617600-163618400	Enhancers	Liver	Liver
7	chr6:163617800-163620400	Weak transcription	Brain Substantia Nigra	brain
8	chr6:163617800-163623800	Weak transcription	Brain Anterior Caudate	brain
9	chr6:163618000-163619400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:163618000-163620400	Weak transcription	Brain Hippocampus Middle	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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