Variant report

Variant	rs12587007
Chromosome Location	chr14:97098734-97098735
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
2	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
3	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11160347	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11160349	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12587582	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12590413	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12590495	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12590511	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17094217	0.98[EUR][1000 genomes]
rs17094229	0.98[EUR][1000 genomes]
rs17094236	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17094246	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17094253	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17094273	0.82[AMR][1000 genomes]
rs17214379	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17214386	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28755993	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56127553	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58362393	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58551820	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58559639	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58652960	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59620844	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60260112	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61170585	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs735408	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs735409	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs74086960	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042409	chr14:96832303-97115668	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv542178	chr14:96832303-97115668	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1048302	chr14:97000845-97250538	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1041078	chr14:97001679-97279220	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1050075	chr14:97004951-97279220	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv431026	chr14:97079926-97163106	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1048209	chr14:97083283-97103070	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv565650	chr14:97089607-97126153	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv470663	chr14:97092803-97127431	Weak transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv565651	chr14:97097653-97137681	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97098400-97100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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