Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12693013	0.88[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12989240	1.00[MEX][hapmap];0.86[MKK][hapmap]
rs1446980	1.00[MEX][hapmap]
rs1559626	1.00[AMR][1000 genomes]
rs1863174	1.00[MEX][hapmap]
rs2081405	1.00[AFR][1000 genomes]
rs2247800	1.00[YRI][hapmap]
rs2357807	1.00[MEX][hapmap]
rs2357950	0.89[AMR][1000 genomes]
rs2432927	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2468393	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2553000	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2553002	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2553003	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2553004	1.00[MEX][hapmap]
rs2553014	1.00[MEX][hapmap]
rs2592938	1.00[MEX][hapmap]
rs2592940	1.00[MEX][hapmap]
rs2676503	1.00[MEX][hapmap]
rs2676509	1.00[AMR][1000 genomes]
rs2676513	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2676516	1.00[MEX][hapmap]
rs2676527	1.00[MEX][hapmap]
rs2884283	1.00[MEX][hapmap]
rs4972866	1.00[MEX][hapmap]
rs6433381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6728322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6728688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6728765	0.82[ASW][hapmap];0.93[MKK][hapmap]

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	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173642600-173669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:173648600-173660800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:173654400-173671400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:173655600-173675600	Weak transcription	Fetal Heart	heart
5	chr2:173656000-173660400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:173656600-173671600	Weak transcription	Brain Angular Gyrus	brain
7	chr2:173657800-173665000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr2:173657800-173671800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:173658000-173660600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:173659400-173671800	Weak transcription	Brain Inferior Temporal Lobe	brain

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