Variant report

Variant	rs16840074
Chromosome Location	chr1:150683156-150683157
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:150674686..150676800-chr1:150681691..150685110,3	K562	blood:
2	chr1:150681352..150684281-chr1:150686110..150688305,2	K562	blood:
3	chr1:150681352..150684293-chr1:150686425..150688305,2	K562	blood:

Variant related genes	Relation type
ENSG00000143452	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1053701	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs10788795	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10888396	0.81[EUR][1000 genomes]
rs11204665	0.91[CEU][hapmap]
rs11204674	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11204689	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11204700	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11204714	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11204715	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11204727	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11576175	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12031458	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12032445	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12034302	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs12038403	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12045807	0.92[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs12728254	0.85[EUR][1000 genomes]
rs1811698	0.83[ASN][1000 genomes]
rs1932864	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2134688	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs3738483	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs3754207	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3768017	0.85[EUR][1000 genomes]
rs3820541	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs3820543	0.85[EUR][1000 genomes]
rs4379678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4970970	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55890313	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61817598	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61817599	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61817600	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6587515	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs6587517	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6661100	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6671703	0.82[EUR][1000 genomes]
rs6679701	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6684611	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6692277	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6696167	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72704624	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7517	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs7517566	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs7520511	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7520516	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7529204	0.82[EUR][1000 genomes]
rs7535975	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7543465	0.91[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006838	chr1:150440214-150722783	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	esv2829859	chr1:150608894-150937329	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv872417	chr1:150618632-150759979	Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv437158	chr1:150652202-150683512	Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150670600-150702600	Weak transcription	Hela-S3	cervix
2	chr1:150679200-150698600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:150681600-150702600	Weak transcription	A549	lung
4	chr1:150682600-150683400	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:150683000-150683400	Weak transcription	K562	blood

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