Variant report

Variant	rs10271908
Chromosome Location	chr7:118659764-118659765
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
2	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10230294	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10242888	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10243067	0.98[ASN][1000 genomes]
rs10259465	0.98[ASN][1000 genomes]
rs10270095	0.98[ASN][1000 genomes]
rs10281568	0.98[ASN][1000 genomes]
rs10480733	0.98[ASN][1000 genomes]
rs10953887	0.98[ASN][1000 genomes]
rs10953893	0.98[ASN][1000 genomes]
rs10953894	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11763344	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12534529	0.98[ASN][1000 genomes]
rs12534565	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12535977	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12671837	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12706217	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12706219	0.98[ASN][1000 genomes]
rs4288311	0.96[ASN][1000 genomes]
rs4295599	0.98[ASN][1000 genomes]
rs4296970	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4310138	0.98[ASN][1000 genomes]
rs4310139	0.98[ASN][1000 genomes]
rs4311606	0.98[ASN][1000 genomes]
rs4320489	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4339573	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4341090	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4341104	0.98[ASN][1000 genomes]
rs4445154	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4490772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4510784	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4512315	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4515483	0.98[ASN][1000 genomes]
rs4523177	0.94[ASN][1000 genomes]
rs4566965	0.98[ASN][1000 genomes]
rs4577886	0.98[ASN][1000 genomes]
rs4617078	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4617095	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4730908	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6466686	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6947555	0.98[ASN][1000 genomes]
rs7788041	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv889096	chr7:118438184-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1021902	chr7:118452600-118719244	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv831110	chr7:118543340-118739362	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv889098	chr7:118590050-118896639	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1016543	chr7:118626169-118660614	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1825159	chr7:118640865-118842361	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2762700	chr7:118658889-118699852	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv981830	chr7:118659625-118667610	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118657800-118666400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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