Variant report

Variant	rs73755069
Chromosome Location	chr6:74543608-74543609
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11992	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs41265543	1.00[EUR][1000 genomes]
rs41266759	1.00[EUR][1000 genomes]
rs45571640	1.00[EUR][1000 genomes]
rs55687737	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56831575	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57686124	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58538884	1.00[EUR][1000 genomes]
rs60516762	1.00[EUR][1000 genomes]
rs6909346	1.00[EUR][1000 genomes]
rs73754673	1.00[ASN][1000 genomes]
rs73754674	1.00[ASN][1000 genomes]
rs73755036	1.00[ASN][1000 genomes]
rs73755064	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73755066	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73755077	1.00[EUR][1000 genomes]
rs73755081	1.00[EUR][1000 genomes]
rs73755082	1.00[EUR][1000 genomes]
rs73755085	1.00[EUR][1000 genomes]
rs7742662	1.00[ASN][1000 genomes]
rs7748689	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9446956	1.00[EUR][1000 genomes]
rs9446969	1.00[EUR][1000 genomes]
rs9446971	1.00[EUR][1000 genomes]
rs9446974	1.00[EUR][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:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74441400-74544400	Weak transcription	Aorta	Aorta
2	chr6:74514400-74545000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:74514400-74546200	Weak transcription	HSMM	muscle
4	chr6:74521800-74545200	Weak transcription	Osteobl	bone
5	chr6:74526400-74565000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr6:74528600-74557000	Weak transcription	Primary T cells from cord blood	blood
7	chr6:74531200-74544000	Weak transcription	NHEK	skin
8	chr6:74531200-74553400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:74531400-74545000	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:74532200-74546800	Weak transcription	HUVEC	blood vessel
11	chr6:74533400-74545000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:74534400-74545400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:74534400-74580600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr6:74538000-74545000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:74539600-74545000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:74540800-74545000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:74541000-74552800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr6:74541400-74543800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:74541800-74543800	Strong transcription	Primary hematopoietic stem cells	blood
20	chr6:74542400-74566800	Weak transcription	HMEC	breast
21	chr6:74542800-74545000	Strong transcription	NHDF-Ad	bronchial
22	chr6:74543000-74545000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:74543600-74543800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:74543600-74551400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:74543600-74553600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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