Variant report

Variant	rs35281010
Chromosome Location	chr3:17138300-17138301
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11128818	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11549706	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13059760	0.89[EUR][1000 genomes]
rs13062572	0.88[EUR][1000 genomes]
rs13073832	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13077235	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13088560	0.82[EUR][1000 genomes]
rs13089569	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13097797	0.89[EUR][1000 genomes]
rs34704046	0.89[EUR][1000 genomes]
rs34937985	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs35185988	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35216408	0.88[EUR][1000 genomes]
rs35545382	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36118680	0.89[EUR][1000 genomes]
rs62247257	0.89[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17129000-17141400	Weak transcription	Fetal Brain Female	brain
2	chr3:17130400-17143400	Weak transcription	Thymus	Thymus
3	chr3:17131200-17143800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr3:17133600-17142600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:17134000-17142600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr3:17134200-17142800	Weak transcription	Primary B cells from peripheral blood	blood

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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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