Variant report

Variant	rs73039324
Chromosome Location	chr1:172036809-172036810
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12058617	1.00[EUR][1000 genomes]
rs16843624	1.00[EUR][1000 genomes]
rs41476749	1.00[EUR][1000 genomes]
rs479185	1.00[EUR][1000 genomes]
rs493630	1.00[EUR][1000 genomes]
rs493657	1.00[EUR][1000 genomes]
rs530846	1.00[EUR][1000 genomes]
rs532194	1.00[EUR][1000 genomes]
rs551742	1.00[EUR][1000 genomes]
rs558496	1.00[EUR][1000 genomes]
rs57282067	1.00[EUR][1000 genomes]
rs57446042	1.00[EUR][1000 genomes]
rs59123048	1.00[EUR][1000 genomes]
rs59949348	1.00[EUR][1000 genomes]
rs609222	1.00[EUR][1000 genomes]
rs642312	1.00[EUR][1000 genomes]
rs650603	1.00[EUR][1000 genomes]
rs654524	1.00[EUR][1000 genomes]
rs73039305	1.00[EUR][1000 genomes]
rs73039329	1.00[AMR][1000 genomes]
rs73039369	1.00[EUR][1000 genomes]
rs73039392	1.00[EUR][1000 genomes]
rs73043064	1.00[EUR][1000 genomes]
rs74126542	1.00[EUR][1000 genomes]
rs74126543	1.00[EUR][1000 genomes]
rs74126545	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	nsv532342	chr1:171922237-172133785	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
2	nsv3532	chr1:171997451-172042351	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172010600-172051400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:172010800-172037600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:172011400-172037800	Weak transcription	Ovary	ovary
4	chr1:172015000-172042600	Weak transcription	Fetal Brain Female	brain
5	chr1:172016600-172037800	Weak transcription	Brain Substantia Nigra	brain
6	chr1:172020200-172038800	Weak transcription	Brain Angular Gyrus	brain
7	chr1:172020200-172040600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:172024600-172040400	Weak transcription	Brain Anterior Caudate	brain
9	chr1:172024800-172040600	Weak transcription	Brain Germinal Matrix	brain
10	chr1:172025200-172037600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr1:172025200-172037800	Weak transcription	Brain Hippocampus Middle	brain
12	chr1:172025200-172040600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:172025400-172037800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr1:172035800-172040400	Weak transcription	Left Ventricle	heart
15	chr1:172036600-172037400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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