Variant report

Variant	rs9473675
Chromosome Location	chr6:13203000-13203001
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11970697	1.00[EUR][1000 genomes]
rs1398299	1.00[EUR][1000 genomes]
rs16873890	1.00[EUR][1000 genomes]
rs16873911	1.00[EUR][1000 genomes]
rs2000372	1.00[EUR][1000 genomes]
rs2000373	1.00[EUR][1000 genomes]
rs2000374	1.00[EUR][1000 genomes]
rs34295856	1.00[EUR][1000 genomes]
rs559205	1.00[EUR][1000 genomes]
rs56796209	1.00[EUR][1000 genomes]
rs56850307	1.00[EUR][1000 genomes]
rs61017997	1.00[EUR][1000 genomes]
rs61059365	1.00[EUR][1000 genomes]
rs6458615	1.00[EUR][1000 genomes]
rs6900887	1.00[EUR][1000 genomes]
rs6901091	1.00[EUR][1000 genomes]
rs6903869	1.00[EUR][1000 genomes]
rs6906831	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6908840	1.00[EUR][1000 genomes]
rs6909931	1.00[EUR][1000 genomes]
rs6910469	1.00[EUR][1000 genomes]
rs6910939	1.00[EUR][1000 genomes]
rs6911906	1.00[EUR][1000 genomes]
rs6913698	1.00[EUR][1000 genomes]
rs6922653	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6923943	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6927426	1.00[EUR][1000 genomes]
rs6936929	1.00[EUR][1000 genomes]
rs73355365	1.00[EUR][1000 genomes]
rs73357154	1.00[EUR][1000 genomes]
rs73357161	1.00[EUR][1000 genomes]
rs73357163	1.00[EUR][1000 genomes]
rs73357179	1.00[EUR][1000 genomes]
rs73357182	1.00[EUR][1000 genomes]
rs73368123	1.00[EUR][1000 genomes]
rs73368194	1.00[EUR][1000 genomes]
rs73725636	1.00[EUR][1000 genomes]
rs73725637	1.00[EUR][1000 genomes]
rs7749076	1.00[EUR][1000 genomes]
rs7767573	1.00[EUR][1000 genomes]
rs7769935	1.00[EUR][1000 genomes]
rs9463350	1.00[EUR][1000 genomes]
rs9463542	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9473216	1.00[EUR][1000 genomes]
rs9473677	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9473688	1.00[EUR][1000 genomes]
rs9473689	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv600992	chr6:12961922-13218549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13178800-13217400	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:13182000-13205400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr6:13182000-13211800	Weak transcription	Fetal Brain Female	brain
4	chr6:13182000-13212000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:13182000-13230000	Weak transcription	Brain Angular Gyrus	brain
6	chr6:13183000-13207000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr6:13184000-13220800	Weak transcription	Brain Germinal Matrix	brain
8	chr6:13185200-13204000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr6:13185200-13205200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:13185400-13204800	Weak transcription	Lung	lung
11	chr6:13185400-13205800	Weak transcription	Aorta	Aorta
12	chr6:13185400-13205800	Weak transcription	Pancreas	Pancrea
13	chr6:13187400-13217400	Weak transcription	Right Atrium	heart
14	chr6:13191200-13204400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:13191800-13210800	Weak transcription	Fetal Heart	heart
16	chr6:13192000-13205600	Weak transcription	Right Ventricle	heart
17	chr6:13192400-13216800	Weak transcription	Fetal Intestine Small	intestine
18	chr6:13193400-13205400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr6:13195600-13205000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr6:13195800-13206200	Weak transcription	Brain Hippocampus Middle	brain
21	chr6:13195800-13207400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:13197600-13203200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:13197800-13204600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr6:13198400-13205200	Weak transcription	Left Ventricle	heart
25	chr6:13198800-13206800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:13201400-13216200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:13201600-13206000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:13201600-13209000	Weak transcription	Ovary	ovary
29	chr6:13201600-13215600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:13202200-13205800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr6:13202400-13213200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:13202400-13218400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:13202800-13207800	Strong transcription	Brain Anterior Caudate	brain
34	chr6:13203000-13203200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:13203000-13203800	Enhancers	K562	blood
36	chr6:13203000-13216800	Weak transcription	Adipose Nuclei	Adipose

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