Variant report

Variant	rs1147538
Chromosome Location	chr6:73274601-73274602
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	chr6:73271338..73274048-chr6:73274112..73275955,2	K562	blood:
2	chr6:73270287..73274048-chr6:73274112..73277683,5	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10085254	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10485210	0.90[EUR][1000 genomes]
rs10485211	0.94[EUR][1000 genomes]
rs1147534	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147536	0.94[EUR][1000 genomes]
rs1147537	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147540	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1202107	1.00[CEU][hapmap]
rs1202110	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1202117	0.94[EUR][1000 genomes]
rs1202118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1202120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1202121	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1202122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1334345	0.83[EUR][1000 genomes]
rs1590801	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16882468	0.87[EUR][1000 genomes]
rs16882473	0.90[EUR][1000 genomes]
rs16882476	0.89[EUR][1000 genomes]
rs16882487	1.00[CEU][hapmap]
rs16882500	1.00[CEU][hapmap]
rs16882506	0.90[EUR][1000 genomes]
rs16882539	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4307137	0.90[EUR][1000 genomes]
rs55739455	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59106883	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59352656	0.90[EUR][1000 genomes]
rs61032405	0.90[EUR][1000 genomes]
rs66805874	0.81[EUR][1000 genomes]
rs68186765	0.90[EUR][1000 genomes]
rs6909267	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72939319	0.87[EUR][1000 genomes]
rs72941783	0.83[EUR][1000 genomes]
rs72941788	0.83[EUR][1000 genomes]
rs72943183	0.90[EUR][1000 genomes]
rs72946182	0.94[EUR][1000 genomes]
rs72946193	0.94[EUR][1000 genomes]
rs72948113	0.94[EUR][1000 genomes]
rs9442816	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9442819	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446697	0.94[EUR][1000 genomes]
rs9446701	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446703	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446704	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446705	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv981067	chr6:73273080-73276402	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73274000-73274800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:73274600-73275200	Enhancers	K562	blood

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