Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10089009	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10093232	0.93[EUR][1000 genomes]
rs10093382	0.80[EUR][1000 genomes]
rs10108248	0.93[EUR][1000 genomes]
rs10955822	0.93[EUR][1000 genomes]
rs10955823	0.87[EUR][1000 genomes]
rs10955825	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1160474	0.83[EUR][1000 genomes]
rs13254406	0.81[EUR][1000 genomes]
rs13280410	0.80[EUR][1000 genomes]
rs13439042	0.83[EUR][1000 genomes]
rs1383176	0.93[EUR][1000 genomes]
rs1396354	0.83[EUR][1000 genomes]
rs1508555	0.80[EUR][1000 genomes]
rs1508566	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1508569	0.86[EUR][1000 genomes]
rs16890041	0.93[EUR][1000 genomes]
rs17753197	0.95[EUR][1000 genomes]
rs218017	0.88[CEU][hapmap];0.83[JPT][hapmap]
rs218018	0.92[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs2202792	0.83[EUR][1000 genomes]
rs2202793	0.83[EUR][1000 genomes]
rs34660998	0.92[EUR][1000 genomes]
rs4604472	0.93[EUR][1000 genomes]
rs6469700	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6469701	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7815693	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7838659	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831438	chr8:118679896-118823600	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv891410	chr8:118684994-118730344	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118684800-118693600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:118685000-118694200	Weak transcription	NHLF	lung
3	chr8:118685200-118690400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:118687000-118689800	Enhancers	NHEK	skin
5	chr8:118687200-118689800	Enhancers	Dnd41	blood
6	chr8:118688800-118690400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:118689000-118690400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:118689000-118694200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:118689200-118690400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:118689200-118692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:118689200-118698200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:118689200-118698600	Weak transcription	HMEC	breast
13	chr8:118689200-118718600	Weak transcription	Osteobl	bone
14	chr8:118689400-118690400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:118689400-118690400	Weak transcription	HSMM	muscle
16	chr8:118689400-118690400	Weak transcription	NHDF-Ad	bronchial
17	chr8:118689400-118695200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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