Variant report

Variant	rs2997697
Chromosome Location	chr9:72714939-72714940
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1927110	0.81[AFR][1000 genomes]
rs2975869	0.89[AFR][1000 genomes]
rs2975870	0.89[AFR][1000 genomes]
rs2975871	0.89[AFR][1000 genomes]
rs2975872	0.87[AFR][1000 genomes]
rs2975873	0.89[AFR][1000 genomes]
rs2975874	0.89[AFR][1000 genomes]
rs2975875	0.87[AFR][1000 genomes]
rs2975876	0.89[AFR][1000 genomes]
rs2975878	0.89[AFR][1000 genomes]
rs2975881	0.89[AFR][1000 genomes]
rs2975882	0.89[AFR][1000 genomes]
rs2975883	0.89[AFR][1000 genomes]
rs2975884	0.81[AFR][1000 genomes]
rs2975885	0.89[AFR][1000 genomes]
rs2975886	0.89[AFR][1000 genomes]
rs2975887	0.89[AFR][1000 genomes]
rs2997683	0.82[AFR][1000 genomes]
rs2997688	0.87[AFR][1000 genomes]
rs2997689	0.87[AFR][1000 genomes]
rs2997691	0.89[AFR][1000 genomes]
rs2997692	0.89[AFR][1000 genomes]
rs2997694	0.89[AFR][1000 genomes]
rs2997695	0.89[AFR][1000 genomes]
rs2997698	0.89[AFR][1000 genomes]
rs2997699	0.89[AFR][1000 genomes]
rs2997700	0.89[AFR][1000 genomes]
rs2997701	0.89[AFR][1000 genomes]
rs2997702	0.89[AFR][1000 genomes]
rs2997703	0.86[AFR][1000 genomes]
rs2997704	0.89[AFR][1000 genomes]
rs2997705	0.89[AFR][1000 genomes]
rs2997706	0.89[AFR][1000 genomes]
rs3015190	0.87[AFR][1000 genomes]
rs3015191	0.89[AFR][1000 genomes]
rs3015193	0.89[AFR][1000 genomes]
rs3015194	0.89[AFR][1000 genomes]
rs3015195	0.89[AFR][1000 genomes]
rs3015196	0.89[AFR][1000 genomes]
rs3015197	0.89[AFR][1000 genomes]
rs3015198	0.81[AFR][1000 genomes]
rs3015199	0.89[AFR][1000 genomes]
rs3015201	0.89[AFR][1000 genomes]
rs3015202	0.89[AFR][1000 genomes]
rs3015203	0.91[AFR][1000 genomes]
rs3015205	0.89[AFR][1000 genomes]
rs3015206	0.89[AFR][1000 genomes]
rs3015208	0.89[AFR][1000 genomes]
rs3015209	0.89[AFR][1000 genomes]
rs3015210	0.89[AFR][1000 genomes]
rs3015212	0.89[AFR][1000 genomes]
rs3015214	0.89[AFR][1000 genomes]
rs3015215	0.89[AFR][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	nsv893438	chr9:72363992-72720438	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1049457	chr9:72539144-72765913	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv831613	chr9:72586058-72740061	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv949052	chr9:72698039-72741247	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72694800-72721400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:72707400-72726800	Weak transcription	Pancreas	Pancrea
3	chr9:72709200-72721400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:72709400-72715200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr9:72709400-72715200	Weak transcription	Fetal Lung	lung
6	chr9:72709400-72722600	Weak transcription	HSMM	muscle
7	chr9:72709600-72715400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:72710200-72715000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr9:72710200-72715200	Weak transcription	Ovary	ovary
10	chr9:72710200-72719000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:72711600-72715200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr9:72711600-72715200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr9:72712400-72718000	Enhancers	Colon Smooth Muscle	Colon
14	chr9:72712600-72716800	Enhancers	Rectal Smooth Muscle	rectum
15	chr9:72712800-72716000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr9:72713200-72723200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:72713600-72715400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr9:72713800-72715200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:72713800-72715600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr9:72713800-72725600	Weak transcription	Stomach Mucosa	stomach
21	chr9:72713800-72728200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr9:72714400-72715800	Strong transcription	HSMMtube	muscle
23	chr9:72714800-72715200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr9:72714800-72742400	Weak transcription	Aorta	Aorta

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