Variant report

Variant	rs10865748
Chromosome Location	chr3:17138332-17138333
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10865747	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4685431	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs55641789	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58238441	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62247258	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62248160	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62248161	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62248162	0.83[EUR][1000 genomes]
rs62248169	0.81[ASN][1000 genomes]
rs62248170	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6808782	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][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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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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