Variant report

Variant	rs60329859
Chromosome Location	chr4:143454630-143454631
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10519649	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11100748	0.84[AMR][1000 genomes]
rs11100749	0.84[AMR][1000 genomes]
rs11930912	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12504375	0.85[AMR][1000 genomes]
rs12504378	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12504770	0.86[AMR][1000 genomes]
rs17717651	0.86[AMR][1000 genomes]
rs2059510	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2059511	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2059513	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs35854467	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs4975306	0.86[AMR][1000 genomes]
rs4975316	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs4975317	0.85[AMR][1000 genomes]
rs4975318	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs61104737	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv461660	chr4:143437219-143538179	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv595605	chr4:143437219-143538179	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143438800-143462800	Weak transcription	Aorta	Aorta
2	chr4:143444400-143456400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr4:143444800-143468400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:143451400-143455400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:143452800-143458800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr4:143453000-143464000	Weak transcription	Fetal Intestine Small	intestine
7	chr4:143453600-143457000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:143453800-143455600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr4:143453800-143458000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:143453800-143459200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:143454600-143459200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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