Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1525497	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16866001	1.00[ASN][1000 genomes]
rs16866005	1.00[ASN][1000 genomes]
rs16866021	1.00[ASN][1000 genomes]
rs17628624	0.84[EUR][1000 genomes]
rs55947224	0.81[EUR][1000 genomes]
rs56083950	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56094154	0.81[EUR][1000 genomes]
rs56151241	0.84[EUR][1000 genomes]
rs56253063	0.81[EUR][1000 genomes]
rs57487804	1.00[ASN][1000 genomes]
rs6739710	1.00[ASN][1000 genomes]
rs72770010	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72770034	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72770043	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72770047	0.84[EUR][1000 genomes]
rs72770054	0.84[EUR][1000 genomes]
rs72770062	0.84[EUR][1000 genomes]
rs72785663	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72785665	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7566298	1.00[ASN][1000 genomes]
rs7574754	0.83[EUR][1000 genomes]
rs7603409	1.00[ASN][1000 genomes]
rs940769	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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1000136	chr2:7337270-7379211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7364400-7369600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr2:7365000-7368200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:7365400-7369000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:7365400-7369400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:7366000-7369600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:7366200-7368400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr2:7366600-7368000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:7367600-7368000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr2:7367600-7368400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr2:7367600-7368400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:7367600-7368600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr2:7367600-7368600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:7367600-7369000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:7367600-7369400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:7367800-7368400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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