Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10269178	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10271713	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10807776	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1860581	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs217542	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs217543	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs217544	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs217582	1.00[ASN][1000 genomes]
rs217583	1.00[ASN][1000 genomes]
rs217586	0.82[EUR][1000 genomes]
rs2191476	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4719427	0.84[CEU][hapmap]
rs4719428	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721379	0.82[CEU][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721381	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6461136	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6461138	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6461139	0.94[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781882	0.83[CEU][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792515	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs978175	0.87[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980013	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr7:14873400-14881200	Weak transcription	NHLF	lung
2	chr7:14875400-14886200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:14876600-14879600	Weak transcription	NHDF-Ad	bronchial
4	chr7:14877000-14879800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:14877000-14880400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:14877000-14880400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:14877000-14880400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:14877000-14881000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:14877000-14883200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:14877000-14886000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:14877200-14880200	Weak transcription	NH-A	brain
12	chr7:14877800-14879800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:14878000-14880600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr7:14878200-14879000	Enhancers	Brain Anterior Caudate	brain
15	chr7:14878200-14882600	Enhancers	Osteobl	bone

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