Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1008290	0.99[ASN][1000 genomes]
rs11767519	0.92[CHB][hapmap]
rs11768553	0.92[CHB][hapmap]
rs11770818	0.92[CHB][hapmap];0.84[JPT][hapmap]
rs11772420	0.92[CHB][hapmap]
rs12155299	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12532038	0.92[CHB][hapmap];0.84[JPT][hapmap]
rs12537983	0.92[CHB][hapmap]
rs12539481	0.92[CHB][hapmap]
rs12706625	0.92[CHB][hapmap];0.84[JPT][hapmap]
rs12706627	0.92[CHB][hapmap]
rs2101100	0.92[CHB][hapmap]
rs2158676	0.99[ASN][1000 genomes]
rs2291207	0.92[CHB][hapmap];0.84[JPT][hapmap]
rs2299904	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs28730874	0.83[ASN][1000 genomes]
rs2896357	0.99[ASN][1000 genomes]
rs4141075	1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs4360236	0.92[CHB][hapmap];0.84[JPT][hapmap]
rs4501522	0.92[CHB][hapmap]
rs4577901	0.99[ASN][1000 genomes]
rs4639456	1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs4728005	1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs6946962	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs6977430	0.99[ASN][1000 genomes]
rs73443822	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7778121	0.84[ASN][1000 genomes]
rs7784168	0.92[CHB][hapmap];0.83[JPT][hapmap]
rs7787804	0.85[CHB][hapmap]
rs7794637	0.92[CHB][hapmap]
rs9641745	0.99[ASN][1000 genomes]

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	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv1027091	chr7:124311742-124388908	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv3446198	chr7:124358002-124586856	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv1802433	chr7:124365503-124385252	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124376800-124389400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr7:124377400-124379200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:124378000-124380600	Enhancers	Brain Substantia Nigra	brain
4	chr7:124378600-124384200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:124378600-124396600	Weak transcription	Fetal Lung	lung
6	chr7:124378800-124379600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:124378800-124382400	Weak transcription	Brain Angular Gyrus	brain
8	chr7:124379000-124380000	Weak transcription	Brain Hippocampus Middle	brain
9	chr7:124379000-124382400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr7:124379000-124382600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:124379000-124386600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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