Variant report

Variant	rs1676052
Chromosome Location	chr14:84552489-84552490
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12435771	0.81[ASN][1000 genomes]
rs12437025	0.84[ASN][1000 genomes]
rs1381614	0.91[ASN][1000 genomes]
rs1462348	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1564057	0.80[ASN][1000 genomes]
rs1766151	0.98[ASN][1000 genomes]
rs1766153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1766155	0.90[ASN][1000 genomes]
rs1766157	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1779555	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779556	0.98[ASN][1000 genomes]
rs1779558	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779559	0.93[ASN][1000 genomes]
rs1779561	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1779562	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1779567	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1779568	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2787459	0.93[ASN][1000 genomes]
rs7146928	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84549600-84554400	Weak transcription	Fetal Heart	heart
2	chr14:84550600-84558400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:84550600-84563800	Weak transcription	Esophagus	oesophagus
4	chr14:84551600-84553800	Weak transcription	Ovary	ovary
5	chr14:84551600-84556800	Weak transcription	Adipose Nuclei	Adipose

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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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