Variant report

Variant	rs6838931
Chromosome Location	chr4:160776756-160776757
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1031637	0.91[ASN][1000 genomes]
rs1031638	0.91[ASN][1000 genomes]
rs12646570	0.93[ASN][1000 genomes]
rs1379601	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1457804	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1457805	0.93[ASN][1000 genomes]
rs17038893	0.87[ASN][1000 genomes]
rs2061337	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2125161	1.00[ASN][1000 genomes]
rs4507315	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4691618	0.87[ASN][1000 genomes]
rs62332987	0.85[ASN][1000 genomes]
rs62332988	0.85[ASN][1000 genomes]
rs62332990	0.87[ASN][1000 genomes]
rs62332991	0.87[ASN][1000 genomes]
rs62332992	0.87[ASN][1000 genomes]
rs62332993	0.82[ASN][1000 genomes]
rs62333020	1.00[ASN][1000 genomes]
rs62333022	0.94[ASN][1000 genomes]
rs62335364	0.85[ASN][1000 genomes]
rs62335365	0.85[ASN][1000 genomes]
rs62335366	0.85[ASN][1000 genomes]
rs6536476	0.87[ASN][1000 genomes]
rs897930	0.91[ASN][1000 genomes]
rs9993289	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv880358	chr4:160694415-161575183	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv595814	chr4:160705097-160834831	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv461696	chr4:160708061-160834831	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv595815	chr4:160708061-160834831	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1029076	chr4:160716044-160841619	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1030555	chr4:160731749-160793323	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv830130	chr4:160748243-160941680	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1027623	chr4:160758359-160837885	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160771000-160783800	Weak transcription	Pancreas	Pancrea
2	chr4:160776400-160777000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links