Variant report

Variant	rs11915692
Chromosome Location	chr3:177388224-177388225
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10513747	0.84[ASN][1000 genomes]
rs10513749	0.81[ASN][1000 genomes]
rs10936953	0.95[ASN][1000 genomes]
rs12487312	0.96[ASN][1000 genomes]
rs12489969	0.95[ASN][1000 genomes]
rs12496321	0.87[ASN][1000 genomes]
rs13059514	0.95[ASN][1000 genomes]
rs13064192	0.80[ASN][1000 genomes]
rs13071785	0.96[ASN][1000 genomes]
rs13074455	0.85[ASN][1000 genomes]
rs13097562	0.81[ASN][1000 genomes]
rs13098037	0.81[ASN][1000 genomes]
rs1499809	0.87[ASN][1000 genomes]
rs1499811	0.83[ASN][1000 genomes]
rs1500048	0.85[ASN][1000 genomes]
rs17635512	0.87[ASN][1000 genomes]
rs17635597	0.85[ASN][1000 genomes]
rs2062500	0.96[ASN][1000 genomes]
rs34066617	0.85[ASN][1000 genomes]
rs34347103	0.85[ASN][1000 genomes]
rs34407557	0.87[ASN][1000 genomes]
rs34491022	0.96[ASN][1000 genomes]
rs34557886	0.87[ASN][1000 genomes]
rs34638059	0.87[ASN][1000 genomes]
rs34763113	0.87[ASN][1000 genomes]
rs35110045	0.87[ASN][1000 genomes]
rs35468531	0.85[ASN][1000 genomes]
rs35610650	0.87[ASN][1000 genomes]
rs35652846	0.87[ASN][1000 genomes]
rs35830472	0.85[ASN][1000 genomes]
rs35847814	0.96[ASN][1000 genomes]
rs36055300	0.87[ASN][1000 genomes]
rs56005554	0.95[ASN][1000 genomes]
rs61541774	0.87[ASN][1000 genomes]
rs66636257	0.87[ASN][1000 genomes]
rs67189039	0.87[ASN][1000 genomes]
rs67797381	0.87[ASN][1000 genomes]
rs68151580	0.96[ASN][1000 genomes]
rs71308158	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752972	chr3:176924298-177425298	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv931055	chr3:177229521-177889872	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv4131	chr3:177366549-177399301	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv10364	chr3:177377030-177390069	ZNF genes & repeats Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv592640	chr3:177383146-177389109	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv33749	chr3:177383470-177389857	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:177383800-177391400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr3:177383800-177397800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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