Variant report

Variant	rs1437579
Chromosome Location	chr6:74542387-74542388
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1109492	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1437576	0.94[TSI][hapmap];0.92[EUR][1000 genomes]
rs1437578	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1437580	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2351530	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2917887	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3005518	0.87[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3012519	0.94[TSI][hapmap];0.92[EUR][1000 genomes]
rs3012541	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3012542	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3012543	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60325463	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61177408	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6925443	0.83[EUR][1000 genomes]
rs6930164	0.83[EUR][1000 genomes];0.81[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	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
2	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
3	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74441400-74544400	Weak transcription	Aorta	Aorta
2	chr6:74477400-74543400	Weak transcription	Lung	lung
3	chr6:74514200-74542800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr6:74514400-74545000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:74514400-74546200	Weak transcription	HSMM	muscle
6	chr6:74521800-74545200	Weak transcription	Osteobl	bone
7	chr6:74526400-74565000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:74528600-74557000	Weak transcription	Primary T cells from cord blood	blood
9	chr6:74531200-74544000	Weak transcription	NHEK	skin
10	chr6:74531200-74553400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:74531400-74545000	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:74532200-74546800	Weak transcription	HUVEC	blood vessel
13	chr6:74533400-74545000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:74534400-74545400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:74534400-74580600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:74536800-74542400	Strong transcription	HMEC	breast
17	chr6:74538000-74545000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:74539600-74543600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:74539600-74545000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:74540000-74543600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:74540800-74545000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:74541000-74552800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr6:74541400-74542600	Enhancers	NHDF-Ad	bronchial
24	chr6:74541400-74543600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:74541400-74543800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:74541600-74542800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:74541800-74542600	Enhancers	Adipose Nuclei	Adipose
28	chr6:74541800-74543800	Strong transcription	Primary hematopoietic stem cells	blood
29	chr6:74542200-74542600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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