Variant report

Variant	rs61865197
Chromosome Location	chr10:37558434-37558435
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10827764	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10827767	0.82[EUR][1000 genomes]
rs10827768	0.82[EUR][1000 genomes]
rs10827769	0.82[EUR][1000 genomes]
rs10827773	0.82[EUR][1000 genomes]
rs11011055	0.93[AMR][1000 genomes]
rs11011066	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11011071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11011080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11011081	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11011091	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11011098	0.82[EUR][1000 genomes]
rs11011099	0.82[EUR][1000 genomes]
rs11011101	0.82[EUR][1000 genomes]
rs11011102	0.82[EUR][1000 genomes]
rs11011103	0.82[EUR][1000 genomes]
rs11011105	0.82[EUR][1000 genomes]
rs11011106	0.82[EUR][1000 genomes]
rs11011113	0.82[EUR][1000 genomes]
rs11011114	0.82[EUR][1000 genomes]
rs11814667	0.82[EUR][1000 genomes]
rs12355499	0.82[EUR][1000 genomes]
rs12355633	0.84[EUR][1000 genomes]
rs12357165	0.84[EUR][1000 genomes]
rs12358280	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12359966	0.82[EUR][1000 genomes]
rs12360325	0.84[EUR][1000 genomes]
rs12765283	1.00[AMR][1000 genomes]
rs12766568	0.82[EUR][1000 genomes]
rs12766884	0.93[AMR][1000 genomes]
rs12775886	1.00[AMR][1000 genomes]
rs12778083	0.82[EUR][1000 genomes]
rs12778104	0.82[EUR][1000 genomes]
rs12783534	0.82[EUR][1000 genomes]
rs1926123	0.82[EUR][1000 genomes]
rs1926124	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2148272	0.82[EUR][1000 genomes]
rs2296591	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2296592	0.82[EUR][1000 genomes]
rs2296593	0.82[EUR][1000 genomes]
rs34191815	0.84[EUR][1000 genomes]
rs34239465	0.82[EUR][1000 genomes]
rs34569813	0.86[EUR][1000 genomes]
rs34572770	0.82[EUR][1000 genomes]
rs35027552	0.82[EUR][1000 genomes]
rs35359976	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35706720	0.82[EUR][1000 genomes]
rs35999186	0.82[EUR][1000 genomes]
rs4450125	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61859281	0.86[EUR][1000 genomes]
rs61859309	0.82[EUR][1000 genomes]
rs61859336	0.82[EUR][1000 genomes]
rs61859337	0.82[EUR][1000 genomes]
rs61859341	0.82[EUR][1000 genomes]
rs61859343	0.81[EUR][1000 genomes]
rs61865173	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61865175	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61866716	1.00[AMR][1000 genomes]
rs6482029	0.82[EUR][1000 genomes]
rs6482032	0.86[EUR][1000 genomes]
rs7069858	0.82[EUR][1000 genomes]
rs7070285	0.81[EUR][1000 genomes]
rs7093136	0.82[EUR][1000 genomes]
rs7093790	0.82[EUR][1000 genomes]
rs7097277	0.82[EUR][1000 genomes]
rs7897685	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7909101	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758213	chr10:37285763-37625699	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2759742	chr10:37285763-37625699	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv831832	chr10:37366131-37563758	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv947605	chr10:37432194-37615294	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1045454	chr10:37512369-37678936	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv2750892	chr10:37525594-37733381	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv982847	chr10:37549675-37560381	Flanking Active TSS Enhancers Weak transcription Active TSS	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	chr10:37558000-37559400	Enhancers	Colon Smooth Muscle	Colon
2	chr10:37558000-37559400	Enhancers	A549	lung

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