Variant report

Variant	rs60765099
Chromosome Location	chr6:119958464-119958465
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11962346	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11965268	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11967252	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11968410	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11970586	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341487	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1341502	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1935105	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56827361	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57181464	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59241522	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59296586	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59476622	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59761384	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59850213	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61015038	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61533190	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61550882	1.00[AMR][1000 genomes];0.84[EUR][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	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv533518	chr6:119712186-119998618	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1027370	chr6:119869409-120056608	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv538431	chr6:119869409-120056608	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119950000-119968600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:119957200-119960600	Enhancers	Dnd41	blood
3	chr6:119957800-119958800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:119957800-119958800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:119957800-119959400	Enhancers	Thymus	Thymus
6	chr6:119957800-119960400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr6:119958000-119959000	Enhancers	Primary hematopoietic stem cells	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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