Variant report

Variant	rs9889750
Chromosome Location	chr17:67010615-67010616
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10048216	1.00[EUR][1000 genomes]
rs10512522	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10512524	1.00[EUR][1000 genomes]
rs10512525	1.00[EUR][1000 genomes]
rs12103695	0.93[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12103736	1.00[EUR][1000 genomes]
rs13342218	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973430	1.00[EUR][1000 genomes]
rs16973507	1.00[EUR][1000 genomes]
rs16973508	0.87[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16973511	1.00[EUR][1000 genomes]
rs16973554	1.00[EUR][1000 genomes]
rs16973575	1.00[EUR][1000 genomes]
rs2058128	1.00[EUR][1000 genomes]
rs28579127	1.00[EUR][1000 genomes]
rs28777976	1.00[EUR][1000 genomes]
rs28851500	1.00[EUR][1000 genomes]
rs3863518	1.00[EUR][1000 genomes]
rs4968991	1.00[EUR][1000 genomes]
rs57920318	1.00[EUR][1000 genomes]
rs58968107	1.00[EUR][1000 genomes]
rs61744800	1.00[EUR][1000 genomes]
rs7216483	1.00[EUR][1000 genomes]
rs7216499	1.00[EUR][1000 genomes]
rs7220968	1.00[EUR][1000 genomes]
rs7222660	1.00[EUR][1000 genomes]
rs72559406	1.00[EUR][1000 genomes]
rs73354278	1.00[EUR][1000 genomes]
rs8065592	1.00[EUR][1000 genomes]
rs8076805	1.00[EUR][1000 genomes]
rs8081075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9890027	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9890160	1.00[EUR][1000 genomes]
rs9890600	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9890654	1.00[EUR][1000 genomes]
rs9890816	1.00[AMR][1000 genomes]
rs9892453	1.00[EUR][1000 genomes]
rs9893173	1.00[EUR][1000 genomes]
rs9894894	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9895934	1.00[EUR][1000 genomes]
rs9899675	0.87[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9899818	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9900211	1.00[EUR][1000 genomes]
rs9901117	1.00[EUR][1000 genomes]
rs9901228	1.00[EUR][1000 genomes]
rs9902715	1.00[EUR][1000 genomes]
rs9908650	1.00[EUR][1000 genomes]
rs9910224	1.00[EUR][1000 genomes]
rs9913052	1.00[EUR][1000 genomes]
rs9914407	1.00[EUR][1000 genomes]
rs9915531	1.00[EUR][1000 genomes]
rs9916254	1.00[EUR][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	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv833526	chr17:66980758-67137034	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66977800-67027400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr17:66989800-67011000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr17:67000200-67044200	Weak transcription	Right Ventricle	heart
4	chr17:67001200-67014600	Strong transcription	Adipose Nuclei	Adipose
5	chr17:67001800-67010800	Weak transcription	Left Ventricle	heart
6	chr17:67002400-67013200	Weak transcription	Fetal Lung	lung
7	chr17:67003800-67030600	Weak transcription	Brain Angular Gyrus	brain
8	chr17:67004000-67023400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr17:67006000-67013200	Weak transcription	Psoas Muscle	Psoas
10	chr17:67007600-67011400	Strong transcription	Liver	Liver
11	chr17:67007600-67016800	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr17:67007600-67042200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr17:67008400-67044000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr17:67009200-67011000	Enhancers	Hela-S3	cervix
15	chr17:67009200-67011000	Enhancers	HUVEC	blood vessel
16	chr17:67009200-67043200	Weak transcription	Pancreas	Pancrea
17	chr17:67009400-67011400	Strong transcription	Fetal Muscle Trunk	muscle
18	chr17:67009400-67012200	Strong transcription	Skeletal Muscle Male	skeletal muscle
19	chr17:67009400-67044000	Weak transcription	Colon Smooth Muscle	Colon
20	chr17:67009600-67011200	Enhancers	HepG2	liver
21	chr17:67009600-67011400	Strong transcription	Fetal Muscle Leg	muscle
22	chr17:67009800-67011600	Strong transcription	Ovary	ovary
23	chr17:67010000-67011000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr17:67010200-67011200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr17:67010400-67041200	Weak transcription	NHDF-Ad	bronchial
26	chr17:67010600-67011600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr17:67010600-67014600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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