Variant report

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

rs_ID	r²[population]
rs1027230	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1027231	1.00[AFR][1000 genomes]
rs1166720	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1166726	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1688088	1.00[AFR][1000 genomes]
rs16969537	1.00[AMR][1000 genomes]
rs16969600	1.00[AMR][1000 genomes]
rs16969678	1.00[AMR][1000 genomes]
rs2631691	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2631716	1.00[AFR][1000 genomes]
rs2631719	1.00[AFR][1000 genomes]
rs2638008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2638011	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4322636	1.00[AMR][1000 genomes]
rs4641712	1.00[AMR][1000 genomes]
rs589137	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs596717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs603993	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs612775	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs621970	0.81[AFR][1000 genomes]
rs623984	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs628076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs639230	1.00[AMR][1000 genomes]
rs653964	0.95[AFR][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	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv832979	chr15:40041928-40218407	Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40040800-40063400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:40052200-40063600	Weak transcription	Brain Angular Gyrus	brain
3	chr15:40053400-40069400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr15:40054400-40069400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:40054600-40062800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:40056200-40063000	Weak transcription	Esophagus	oesophagus
7	chr15:40058200-40063000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:40058200-40063200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr15:40059000-40063000	Weak transcription	Right Atrium	heart
10	chr15:40059400-40074400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr15:40060200-40063000	Weak transcription	Fetal Stomach	stomach
12	chr15:40060400-40063000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:40060400-40063400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:40060600-40063000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr15:40062600-40063400	Enhancers	NHDF-Ad	bronchial
16	chr15:40062600-40063800	Enhancers	NHLF	lung

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