Variant report

Variant	rs4897438
Chromosome Location	chr6:130899369-130899370
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12665689	0.85[ASN][1000 genomes]
rs1316493	0.94[ASN][1000 genomes]
rs1316537	0.94[ASN][1000 genomes]
rs1316538	0.94[ASN][1000 genomes]
rs1317232	0.94[ASN][1000 genomes]
rs1933757	0.94[ASN][1000 genomes]
rs2326913	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4895886	0.94[ASN][1000 genomes]
rs4895887	0.90[ASN][1000 genomes]
rs4897437	0.94[ASN][1000 genomes]
rs4897439	0.81[AMR][1000 genomes]
rs56019502	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62431565	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62431566	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6569690	0.93[ASN][1000 genomes]
rs6899678	0.96[ASN][1000 genomes]
rs6932512	0.89[ASN][1000 genomes]
rs72988212	0.81[AMR][1000 genomes]
rs7451336	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7452034	0.96[ASN][1000 genomes]
rs7744825	0.94[ASN][1000 genomes]
rs7754423	0.98[ASN][1000 genomes]
rs9321234	0.82[ASN][1000 genomes]
rs9321236	0.80[ASN][1000 genomes]
rs9321238	0.95[ASN][1000 genomes]
rs9321239	0.95[ASN][1000 genomes]
rs9321241	0.95[ASN][1000 genomes]
rs9372966	0.94[ASN][1000 genomes]
rs9372967	0.94[ASN][1000 genomes]
rs9375740	0.94[ASN][1000 genomes]
rs9375741	0.94[ASN][1000 genomes]
rs9402246	0.91[ASN][1000 genomes]
rs9402247	0.94[ASN][1000 genomes]
rs9402248	0.94[ASN][1000 genomes]
rs9483145	0.95[ASN][1000 genomes]
rs9492649	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv427767	chr6:130875056-131008620	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv5475	chr6:130880169-130924850	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130895200-130900000	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr6:130895800-130899400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr6:130896000-130899400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr6:130896000-130899800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr6:130898000-130899800	Enhancers	Dnd41	blood
6	chr6:130898600-130899800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr6:130898800-130899400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr6:130898800-130900000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:130899000-130900000	Enhancers	Primary T cells from cord blood	blood
10	chr6:130899000-130900000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr6:130899000-130900000	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr6:130899000-130900200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr6:130899200-130900000	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr6:130899200-130900400	Enhancers	Liver	Liver

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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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