Variant report

Variant	rs16849508
Chromosome Location	chr4:74364458-74364459
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74358528..74361242-chr4:74363889..74365754,3	K562	blood:
2	chr4:74358528..74361754-chr4:74363889..74365476,3	K562	blood:

Variant related genes	Relation type
ENSG00000079557	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10002756	0.84[JPT][hapmap]
rs10028196	0.84[ASN][1000 genomes]
rs10028276	0.82[ASN][1000 genomes]
rs10212657	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10213305	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10518116	0.85[CEU][hapmap]
rs10805065	0.85[ASN][1000 genomes]
rs10938075	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10938077	0.85[ASN][1000 genomes]
rs10938078	0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs10938079	0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1158101	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1159624	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11733262	0.81[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11935001	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11939341	0.82[ASN][1000 genomes]
rs12504448	0.85[ASN][1000 genomes]
rs12510629	0.85[ASN][1000 genomes]
rs12510870	0.90[CEU][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13103378	0.85[ASN][1000 genomes]
rs13107306	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13120998	0.85[ASN][1000 genomes]
rs13124940	0.82[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs13150405	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1358592	0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1528924	0.81[ASN][1000 genomes]
rs1590115	0.84[ASN][1000 genomes]
rs1590116	0.84[ASN][1000 genomes]
rs16849461	0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16849484	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1894293	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1919479	0.84[ASN][1000 genomes]
rs1997332	0.90[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1997333	0.85[ASN][1000 genomes]
rs2040354	0.85[ASN][1000 genomes]
rs2071097	0.85[ASN][1000 genomes]
rs2071098	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2141465	0.85[ASN][1000 genomes]
rs2141470	0.82[ASN][1000 genomes]
rs2178290	0.85[ASN][1000 genomes]
rs2178292	0.84[ASN][1000 genomes]
rs2204736	0.84[ASN][1000 genomes]
rs34238679	0.81[ASN][1000 genomes]
rs34400902	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34468776	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35233345	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35858007	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35988516	0.86[ASN][1000 genomes]
rs3765639	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3822100	0.81[JPT][hapmap]
rs4235119	0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs4267703	0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs4267704	0.85[ASN][1000 genomes]
rs4267705	0.85[ASN][1000 genomes]
rs4438732	0.84[ASN][1000 genomes]
rs4618279	0.84[ASN][1000 genomes]
rs4631010	0.81[ASN][1000 genomes]
rs4640638	0.81[JPT][hapmap]
rs4694173	0.84[ASN][1000 genomes]
rs56011127	0.84[ASN][1000 genomes]
rs56384466	0.84[ASN][1000 genomes]
rs6446937	0.81[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6446938	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6446939	0.86[ASN][1000 genomes]
rs6446941	0.82[ASN][1000 genomes]
rs6834059	0.81[JPT][hapmap]
rs6852149	0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs6852772	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72647083	0.84[ASN][1000 genomes]
rs7660680	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74353000-74364800	Weak transcription	Fetal Intestine Small	intestine
2	chr4:74354000-74365600	Weak transcription	Fetal Intestine Large	intestine
3	chr4:74361800-74371800	Genic enhancers	Liver	Liver
4	chr4:74364200-74364800	Enhancers	K562	blood

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