Variant report

Variant	rs73612461
Chromosome Location	chr6:150227134-150227135
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:17)

rs_ID	r²[population]
rs3860813	1.00[AMR][1000 genomes]
rs56706316	1.00[AMR][1000 genomes]
rs56896927	1.00[AMR][1000 genomes]
rs57472228	1.00[AMR][1000 genomes]
rs58307895	1.00[AMR][1000 genomes]
rs58946697	1.00[AMR][1000 genomes]
rs59281875	1.00[AMR][1000 genomes]
rs59878448	1.00[AMR][1000 genomes]
rs60248818	1.00[AMR][1000 genomes]
rs60386924	1.00[AMR][1000 genomes]
rs60494754	1.00[AMR][1000 genomes]
rs60897658	1.00[AMR][1000 genomes]
rs61084626	1.00[AMR][1000 genomes]
rs61230059	1.00[AMR][1000 genomes]
rs61285074	1.00[AMR][1000 genomes]
rs73612479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7748726	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886764	chr6:150114745-150393683	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription 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	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv886765	chr6:150198491-150288722	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1817805	chr6:150209592-150268708	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr6:150218800-150227600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:150222600-150229800	Weak transcription	Pancreas	Pancrea
3	chr6:150225200-150227400	Enhancers	Fetal Muscle Leg	muscle
4	chr6:150225400-150227200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr6:150225400-150227600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr6:150225400-150227800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr6:150226000-150227800	Enhancers	Lung	lung
8	chr6:150226200-150227400	Weak transcription	Right Atrium	heart
9	chr6:150226200-150242000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:150226400-150227600	Enhancers	Left Ventricle	heart
11	chr6:150226400-150227800	Enhancers	Right Ventricle	heart
12	chr6:150226600-150227200	Enhancers	Esophagus	oesophagus
13	chr6:150226600-150227400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:150226600-150228200	Enhancers	Adipose Nuclei	Adipose
15	chr6:150227000-150227200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:150227000-150227200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:150227000-150227800	Enhancers	Spleen	Spleen

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Input of quick search could be:

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

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