Variant report

Variant	rs1618834
Chromosome Location	chr6:38778285-38778286
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1615441	0.84[EUR][1000 genomes]
rs1616105	0.84[EUR][1000 genomes]
rs1617807	0.84[EUR][1000 genomes]
rs1618774	0.84[EUR][1000 genomes]
rs1622275	0.85[ASN][1000 genomes]
rs1627917	0.84[EUR][1000 genomes]
rs1678664	0.82[ASN][1000 genomes]
rs1678666	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1678674	0.90[ASN][1000 genomes]
rs1678676	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1678686	0.85[ASN][1000 genomes]
rs1678710	0.84[EUR][1000 genomes]
rs1678711	0.84[EUR][1000 genomes]
rs1678716	0.84[EUR][1000 genomes]
rs1678719	0.84[EUR][1000 genomes]
rs1678720	0.84[EUR][1000 genomes]
rs1678721	0.84[EUR][1000 genomes]
rs1678722	0.84[EUR][1000 genomes]
rs1678724	0.84[EUR][1000 genomes]
rs1678728	0.84[EUR][1000 genomes]
rs1678729	0.84[EUR][1000 genomes]
rs1678730	0.84[EUR][1000 genomes]
rs1678731	0.84[EUR][1000 genomes]
rs1678732	0.84[EUR][1000 genomes]
rs1678733	0.84[EUR][1000 genomes]
rs1678734	0.84[EUR][1000 genomes]
rs1678735	0.84[EUR][1000 genomes]
rs1738200	0.84[EUR][1000 genomes]
rs1738202	0.83[EUR][1000 genomes]
rs1738206	0.84[EUR][1000 genomes]
rs1738207	0.84[EUR][1000 genomes]
rs1738208	0.84[EUR][1000 genomes]
rs1738209	0.84[EUR][1000 genomes]
rs1738210	0.84[EUR][1000 genomes]
rs1738213	0.84[EUR][1000 genomes]
rs1738214	0.84[EUR][1000 genomes]
rs1738224	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1738226	0.85[ASN][1000 genomes]
rs1738233	0.93[ASN][1000 genomes]
rs1738234	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1738237	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1738242	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1738246	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1738249	0.87[ASN][1000 genomes]
rs6912563	0.85[ASN][1000 genomes]
rs6928298	0.84[ASN][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	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv830642	chr6:38645056-38800657	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv830643	chr6:38726675-38905589	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv602959	chr6:38728142-38786528	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv470814	chr6:38728142-38790149	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv462916	chr6:38747770-38782401	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv602960	chr6:38747770-38782401	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription	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	chr6:38766800-38824400	Weak transcription	K562	blood
2	chr6:38775000-38779000	Weak transcription	GM12878-XiMat	blood

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