Variant report

Variant	rs4763316
Chromosome Location	chr12:9936313-9936314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10844765	0.84[EUR][1000 genomes]
rs10844769	0.83[AFR][1000 genomes]
rs10844780	0.99[EUR][1000 genomes]
rs10844781	0.99[EUR][1000 genomes]
rs10844782	0.99[EUR][1000 genomes]
rs11053051	0.99[EUR][1000 genomes]
rs12301123	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12314225	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12822701	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12824491	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2110449	0.82[AFR][1000 genomes]
rs2110450	0.84[AFR][1000 genomes]
rs2160087	0.84[AFR][1000 genomes]
rs4763315	0.96[EUR][1000 genomes]
rs4763317	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7958591	0.84[AFR][1000 genomes]
rs7964603	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7972330	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9927600-9938800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:9928400-9945400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:9930000-9945400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:9930200-9945800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:9934400-9938400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:9934600-9937600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:9934600-9938200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:9934600-9939800	Weak transcription	Primary T cells from cord blood	blood
9	chr12:9934600-9940000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr12:9935200-9941200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:9935400-9936600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:9935400-9938000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr12:9935400-9940400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:9935600-9937400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr12:9935800-9936800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr12:9936000-9936400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr12:9936000-9941000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:9936200-9937200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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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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