Variant report

Variant	rs4763932
Chromosome Location	chr12:9940994-9940995
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10772147	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11053116	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12301753	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2110448	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2401400	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2401401	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4763931	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4763935	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488204	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7966635	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7975116	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3377937	chr12:9938734-9962518	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9928400-9945400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:9930000-9945400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr12:9930200-9945800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr12:9935200-9941200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:9936000-9941000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:9937600-9941000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr12:9937800-9941000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr12:9939000-9945200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:9939800-9941000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr12:9939800-9943600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr12:9939800-9943800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:9939800-9945000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr12:9940600-9945000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr12:9940600-9945000	Weak transcription	NH-A	brain
15	chr12:9940600-9945400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr12:9940800-9941000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:9940800-9942600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:9940800-9945200	Weak transcription	Primary T helper cells fromperipheralblood	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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