Variant report

Variant	rs41266759
Chromosome Location	chr6:74534447-74534448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs41265543	1.00[EUR][1000 genomes]
rs45571640	1.00[EUR][1000 genomes]
rs55687737	1.00[EUR][1000 genomes]
rs58538884	1.00[EUR][1000 genomes]
rs60516762	1.00[EUR][1000 genomes]
rs6909346	1.00[EUR][1000 genomes]
rs6930349	1.00[EUR][1000 genomes]
rs73755069	1.00[EUR][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]
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:39 , 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	chr6:74484600-74542000	Weak transcription	Right Ventricle	heart
4	chr6:74513800-74539600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:74514200-74535400	Weak transcription	NHLF	lung
6	chr6:74514200-74542800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr6:74514400-74545000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:74514400-74546200	Weak transcription	HSMM	muscle
9	chr6:74516400-74535000	Strong transcription	NHDF-Ad	bronchial
10	chr6:74521800-74536000	Weak transcription	Left Ventricle	heart
11	chr6:74521800-74541800	Weak transcription	Adipose Nuclei	Adipose
12	chr6:74521800-74545200	Weak transcription	Osteobl	bone
13	chr6:74524600-74535000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:74525200-74535800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:74526000-74535600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:74526400-74542200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr6:74526400-74565000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr6:74526600-74535600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr6:74527800-74541000	Weak transcription	Esophagus	oesophagus
20	chr6:74528600-74557000	Weak transcription	Primary T cells from cord blood	blood
21	chr6:74530800-74535000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:74531000-74541800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr6:74531200-74536000	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr6:74531200-74544000	Weak transcription	NHEK	skin
25	chr6:74531200-74553400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:74531400-74535800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:74531400-74539600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:74531400-74545000	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:74531600-74541600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr6:74532200-74546800	Weak transcription	HUVEC	blood vessel
31	chr6:74533400-74535400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:74533400-74545000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:74533600-74540800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr6:74533800-74535800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:74534400-74536800	Weak transcription	HMEC	breast
36	chr6:74534400-74539600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:74534400-74540000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:74534400-74545400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:74534400-74580600	Weak transcription	Placenta Amnion	Placenta Amnion

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