Variant report

Variant	rs17118222
Chromosome Location	chr14:47702133-47702134
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10483578	0.94[ASN][1000 genomes]
rs10483579	0.94[ASN][1000 genomes]
rs10484193	0.91[ASN][1000 genomes]
rs12433937	0.94[ASN][1000 genomes]
rs12436030	0.84[ASN][1000 genomes]
rs1571104	0.94[ASN][1000 genomes]
rs17118145	0.91[ASN][1000 genomes]
rs17118150	0.91[ASN][1000 genomes]
rs17118178	0.97[ASN][1000 genomes]
rs17118182	0.97[ASN][1000 genomes]
rs17118191	0.97[ASN][1000 genomes]
rs17118197	0.97[ASN][1000 genomes]
rs17118216	0.94[ASN][1000 genomes]
rs17118298	0.94[ASN][1000 genomes]
rs17653818	1.00[ASN][1000 genomes]
rs17670956	1.00[ASN][1000 genomes]
rs17671662	0.94[ASN][1000 genomes]
rs17671826	0.94[ASN][1000 genomes]
rs17671953	0.94[ASN][1000 genomes]
rs17672024	0.94[ASN][1000 genomes]
rs17739532	0.94[ASN][1000 genomes]
rs17739605	0.94[ASN][1000 genomes]
rs17739629	0.94[ASN][1000 genomes]
rs17739955	0.84[ASN][1000 genomes]
rs17739979	0.94[ASN][1000 genomes]
rs2899997	0.86[ASN][1000 genomes]
rs36117017	0.97[ASN][1000 genomes]
rs55682943	0.91[ASN][1000 genomes]
rs55928353	0.91[ASN][1000 genomes]
rs56159600	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6572410	0.91[ASN][1000 genomes]
rs7142595	0.91[ASN][1000 genomes]
rs7151248	0.94[ASN][1000 genomes]
rs7152122	0.94[ASN][1000 genomes]
rs7152633	0.94[ASN][1000 genomes]
rs72680230	0.94[ASN][1000 genomes]
rs72680232	0.91[ASN][1000 genomes]
rs72680241	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72680244	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680246	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680257	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680259	0.84[EUR][1000 genomes]
rs72680268	1.00[ASN][1000 genomes]
rs72680273	1.00[ASN][1000 genomes]
rs72680274	1.00[ASN][1000 genomes]
rs72680276	1.00[ASN][1000 genomes]
rs72680278	1.00[ASN][1000 genomes]
rs72680280	1.00[ASN][1000 genomes]
rs72680281	1.00[ASN][1000 genomes]
rs72682175	0.94[ASN][1000 genomes]
rs72682176	0.94[ASN][1000 genomes]
rs72682179	0.91[ASN][1000 genomes]
rs72682197	0.94[ASN][1000 genomes]
rs72683803	0.84[ASN][1000 genomes]
rs72683805	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040847	chr14:46905206-47869359	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv542085	chr14:46905206-47869359	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1049865	chr14:46905406-47869220	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv542087	chr14:46905406-47869220	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1048316	chr14:47297113-47885723	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv901890	chr14:47594099-47729711	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv901891	chr14:47620548-47708397	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv901892	chr14:47620548-47729711	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1046326	chr14:47629646-47845903	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv901893	chr14:47633066-47715509	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv456302	chr14:47650921-47715621	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv564772	chr14:47650921-47715621	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv564773	chr14:47697802-47717798	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv976857	chr14:47699994-47704677	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47699200-47703600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr14:47699400-47703000	Weak transcription	HUVEC	blood vessel
3	chr14:47699400-47703600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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