Variant report

Variant	rs17028785
Chromosome Location	chr4:153189533-153189534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10030608	1.00[AMR][1000 genomes]
rs10517564	0.85[LWK][hapmap];0.82[AFR][1000 genomes]
rs17028774	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17028780	0.85[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17028782	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17028792	0.84[AFR][1000 genomes]
rs17028905	1.00[AMR][1000 genomes]
rs4443256	1.00[AMR][1000 genomes]
rs56951677	1.00[AMR][1000 genomes]
rs57378045	1.00[AMR][1000 genomes]
rs58298033	1.00[AMR][1000 genomes]
rs58467748	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58995086	1.00[AMR][1000 genomes]
rs72719909	0.82[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:153187800-153190000	Enhancers	NHEK	skin
2	chr4:153188200-153199400	Weak transcription	Right Atrium	heart
3	chr4:153189000-153194400	Weak transcription	HMEC	breast
4	chr4:153189200-153193600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:153189400-153193800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:153189400-153194600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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