Variant report

Variant	rs10274814
Chromosome Location	chr7:84446946-84446947
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:84445226..84448615-chr7:84449710..84452993,3	K562	blood:
2	chr7:84436641..84439524-chr7:84444759..84447374,2	K562	blood:

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10085820	0.92[AFR][1000 genomes]
rs10225298	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10225557	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10226288	0.92[AFR][1000 genomes]
rs10226313	0.89[AFR][1000 genomes]
rs10227472	0.92[AFR][1000 genomes]
rs10229365	0.92[AFR][1000 genomes]
rs10229476	0.92[AFR][1000 genomes]
rs10229726	0.92[AFR][1000 genomes]
rs10230012	0.92[AFR][1000 genomes]
rs10231227	0.92[AFR][1000 genomes]
rs10234993	0.92[AFR][1000 genomes]
rs10235044	0.92[AFR][1000 genomes]
rs10238680	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10239054	0.92[AFR][1000 genomes]
rs10241357	0.92[AFR][1000 genomes]
rs10242005	0.92[AFR][1000 genomes]
rs10243021	0.92[AFR][1000 genomes]
rs10243755	0.92[AFR][1000 genomes]
rs10243828	0.92[AFR][1000 genomes]
rs10243859	0.92[AFR][1000 genomes]
rs10244922	0.92[AFR][1000 genomes]
rs10250111	0.92[AFR][1000 genomes]
rs10252528	0.92[AFR][1000 genomes]
rs10252836	0.92[AFR][1000 genomes]
rs10253565	0.92[AFR][1000 genomes]
rs10253819	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10254493	0.92[AFR][1000 genomes]
rs10254761	0.88[ASN][1000 genomes]
rs10256352	0.92[AFR][1000 genomes]
rs10257078	0.92[AFR][1000 genomes]
rs10260523	0.92[AFR][1000 genomes]
rs10264147	0.92[AFR][1000 genomes]
rs10265448	0.88[ASN][1000 genomes]
rs10268505	0.92[AFR][1000 genomes]
rs10269671	0.85[AFR][1000 genomes]
rs10271353	0.92[AFR][1000 genomes]
rs10271605	0.92[AFR][1000 genomes]
rs10273534	0.92[AFR][1000 genomes]
rs10273650	0.92[AFR][1000 genomes]
rs10276443	0.92[AFR][1000 genomes]
rs10279991	0.85[AFR][1000 genomes]
rs10282093	0.92[AFR][1000 genomes]
rs1318546	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13437628	0.88[ASN][1000 genomes]
rs13438389	0.92[AFR][1000 genomes]
rs1406341	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1583146	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1594395	1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17159219	1.00[EUR][1000 genomes]
rs17159404	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1811353	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1835402	0.85[AFR][1000 genomes]
rs1864526	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1864527	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1897156	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1997302	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2293574	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28457219	0.92[AFR][1000 genomes]
rs28503172	0.92[AFR][1000 genomes]
rs28576399	0.85[AFR][1000 genomes]
rs28667540	0.92[AFR][1000 genomes]
rs4128623	0.87[ASN][1000 genomes]
rs4236672	1.00[EUR][1000 genomes]
rs4283991	1.00[EUR][1000 genomes]
rs4283992	0.82[ASN][1000 genomes]
rs4286890	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4338048	1.00[EUR][1000 genomes]
rs4398846	0.92[AFR][1000 genomes]
rs4549716	1.00[EUR][1000 genomes]
rs4551285	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4563832	0.86[ASN][1000 genomes]
rs4595076	1.00[EUR][1000 genomes]
rs4621727	0.85[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes]
rs4623351	0.85[JPT][hapmap];1.00[EUR][1000 genomes]
rs4728558	1.00[EUR][1000 genomes]
rs4728568	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4732572	1.00[EUR][1000 genomes]
rs4732574	1.00[EUR][1000 genomes]
rs4732583	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4732584	0.86[ASN][1000 genomes]
rs4732585	0.86[ASN][1000 genomes]
rs4732587	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4732590	1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4732591	1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4732592	1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs58079066	0.80[AMR][1000 genomes]
rs58836788	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59138424	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59348972	0.88[ASN][1000 genomes]
rs59572545	0.92[AFR][1000 genomes]
rs61463020	1.00[EUR][1000 genomes]
rs73710992	1.00[EUR][1000 genomes]
rs73713541	0.89[ASN][1000 genomes]
rs73713553	0.88[ASN][1000 genomes]
rs73713556	0.88[ASN][1000 genomes]
rs934302	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9656563	0.92[AFR][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	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv888641	chr7:84168615-84453100	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv888643	chr7:84196258-84453100	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv831049	chr7:84277599-84475710	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv34238	chr7:84279023-84591966	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv831050	chr7:84355996-84527261	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84439600-84450000	Weak transcription	K562	blood

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