Variant report

Variant	rs4749063
Chromosome Location	chr10:25983691-25983692
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10764579	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10828844	0.83[EUR][1000 genomes]
rs10828846	0.81[EUR][1000 genomes]
rs10828848	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10828849	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11014679	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12242832	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17737307	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2290167	0.95[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2367978	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4749059	0.85[EUR][1000 genomes]
rs6482511	0.88[ASN][1000 genomes]
rs7093919	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7902742	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7908814	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7916640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs989622	0.81[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25962800-25993600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:25978400-25985600	Enhancers	Primary B cells from peripheral blood	blood
3	chr10:25980200-25985600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr10:25980800-25985200	Enhancers	Primary B cells from cord blood	blood
5	chr10:25980800-25990000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr10:25983200-25983800	Enhancers	Placenta	Placenta
7	chr10:25983200-25984400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:25983400-25984400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:25983600-25984000	Enhancers	Primary hematopoietic stem cells	blood
10	chr10:25983600-25984200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr10:25983600-25984600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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