Variant report

Variant	rs2764665
Chromosome Location	chr1:57742783-57742784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1149628	0.85[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1424473	0.88[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1910690	0.90[ASN][1000 genomes]
rs197625	0.88[ASN][1000 genomes]
rs197626	0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs197638	0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs197644	0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs197645	0.88[ASN][1000 genomes]
rs197649	0.90[ASN][1000 genomes]
rs2251472	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs2432690	0.84[EUR][1000 genomes]
rs2656093	0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2656094	0.91[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2656095	0.81[JPT][hapmap]
rs2764664	0.85[MEX][hapmap]
rs486809	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs487566	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs488405	0.90[ASN][1000 genomes]
rs492781	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.98[ASN][1000 genomes]
rs492905	0.90[ASN][1000 genomes]
rs493846	0.90[ASN][1000 genomes]
rs499397	0.91[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs511707	0.81[JPT][hapmap]
rs515802	0.90[ASN][1000 genomes]
rs529527	0.88[ASN][1000 genomes]
rs537441	0.83[ASN][1000 genomes]
rs539229	0.87[ASN][1000 genomes]
rs542873	0.91[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs542949	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs545671	0.84[EUR][1000 genomes]
rs561531	0.81[JPT][hapmap]
rs572092	0.91[CHB][hapmap];0.86[CHD][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs576038	0.84[EUR][1000 genomes]
rs584147	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs587046	0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs593154	0.90[ASN][1000 genomes]
rs595513	0.84[GIH][hapmap];0.95[MEX][hapmap];0.83[TSI][hapmap]
rs595568	0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs596784	0.86[MEX][hapmap]
rs597941	0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs611276	0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs614488	0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs620214	0.91[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs627489	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs627550	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs627936	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs634391	0.80[GIH][hapmap];0.81[JPT][hapmap];0.81[MEX][hapmap]
rs642526	0.81[JPT][hapmap];0.84[EUR][1000 genomes]
rs643382	0.84[GIH][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap]
rs648607	0.86[MEX][hapmap]
rs655277	0.90[ASN][1000 genomes]
rs657612	0.96[ASN][1000 genomes]
rs659069	0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs663975	0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.83[TSI][hapmap];0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs66894620	0.86[ASN][1000 genomes]
rs669931	0.87[ASN][1000 genomes]
rs674966	0.85[MEX][hapmap]
rs675075	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs686702	0.90[ASN][1000 genomes]
rs693942	0.88[ASN][1000 genomes]
rs706385	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.86[AMR][1000 genomes];0.98[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	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2754702	chr1:57716116-57743244	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57735200-57747200	Weak transcription	Esophagus	oesophagus
2	chr1:57737400-57746800	Weak transcription	Fetal Brain Female	brain
3	chr1:57737600-57744200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:57741800-57749400	Enhancers	Fetal Intestine Small	intestine
5	chr1:57742000-57749200	Enhancers	Liver	Liver
6	chr1:57742200-57755400	Weak transcription	Fetal Brain Male	brain
7	chr1:57742400-57743400	Enhancers	Duodenum Mucosa	Duodenum
8	chr1:57742600-57743000	Weak transcription	Fetal Intestine Large	intestine

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