Variant report

Variant	rs13293217
Chromosome Location	chr9:96082919-96082920
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:96072987..96083429-chr9:96209751..96218385,15	MCF-7	breast:

Variant related genes	Relation type
ENSG00000188938	Chromatin interaction
ENSG00000048828	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10761203	0.88[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.87[ASN][1000 genomes]
rs10821080	0.85[CEU][hapmap];0.91[MEX][hapmap]
rs10821086	0.92[CEU][hapmap];0.83[MEX][hapmap]
rs10821088	0.85[CEU][hapmap]
rs10821095	0.85[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs10821098	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.86[ASN][1000 genomes]
rs10992698	0.95[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs10992702	0.92[ASN][1000 genomes]
rs12336667	0.85[CEU][hapmap];0.83[MEX][hapmap]
rs12341303	0.85[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.84[ASN][1000 genomes]
rs12684394	0.89[ASN][1000 genomes]
rs1317698	0.89[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.88[ASN][1000 genomes]
rs13292831	0.88[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2040093	0.92[CEU][hapmap]
rs2040094	0.92[CEU][hapmap]
rs2086103	0.95[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs2306183	0.88[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.88[ASN][1000 genomes]
rs2398822	0.83[ASN][1000 genomes]
rs3001450	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3001451	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35795732	0.86[ASN][1000 genomes]
rs3763634	0.94[CHB][hapmap];0.88[ASN][1000 genomes]
rs3763635	0.88[ASN][1000 genomes]
rs3793546	0.85[ASN][1000 genomes]
rs4743911	0.83[CEU][hapmap];0.88[ASN][1000 genomes]
rs4744195	0.85[CEU][hapmap];0.87[CHB][hapmap];0.88[CHD][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.82[ASN][1000 genomes]
rs4744201	0.84[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.87[ASN][1000 genomes]
rs4744206	0.89[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs4744212	0.89[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs4744215	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs7846729	0.85[CEU][hapmap]
rs7857039	0.96[CEU][hapmap]
rs7857937	0.92[CEU][hapmap];0.83[MEX][hapmap]
rs7868971	0.85[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs944993	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv430082	chr9:95905745-96095045	Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv893582	chr9:95963114-96116937	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893583	chr9:95996573-96091688	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv893584	chr9:96002983-96116937	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96063800-96088600	Weak transcription	Right Atrium	heart
2	chr9:96067600-96086800	Weak transcription	Fetal Brain Male	brain
3	chr9:96067800-96086800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr9:96068200-96086200	Weak transcription	Brain Anterior Caudate	brain
5	chr9:96068400-96100400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:96070600-96087800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr9:96074000-96088600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr9:96076200-96088400	Weak transcription	A549	lung
9	chr9:96077000-96083800	Strong transcription	Duodenum Mucosa	Duodenum
10	chr9:96077000-96085200	Strong transcription	Fetal Brain Female	brain
11	chr9:96079000-96083800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:96079000-96084600	Strong transcription	Fetal Intestine Small	intestine
13	chr9:96079200-96088600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr9:96079600-96094400	Weak transcription	Stomach Mucosa	stomach
15	chr9:96080400-96087200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:96080400-96090400	Weak transcription	Gastric	stomach
17	chr9:96080800-96088000	Weak transcription	Right Ventricle	heart
18	chr9:96081000-96083400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr9:96081000-96086200	Weak transcription	HepG2	liver
20	chr9:96081000-96100600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr9:96081200-96083600	Weak transcription	Spleen	Spleen
22	chr9:96081200-96083800	Enhancers	Fetal Heart	heart
23	chr9:96081200-96088000	Weak transcription	Left Ventricle	heart
24	chr9:96081600-96088000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr9:96081800-96088000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr9:96082000-96083200	Enhancers	Fetal Muscle Leg	muscle
27	chr9:96082000-96083600	Enhancers	Fetal Lung	lung
28	chr9:96082000-96083800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:96082000-96083800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:96082200-96083200	Enhancers	Fetal Muscle Trunk	muscle
31	chr9:96082200-96085400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr9:96082200-96086400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr9:96082400-96083800	Strong transcription	Stomach Smooth Muscle	stomach
34	chr9:96082400-96084800	Weak transcription	Colonic Mucosa	Colon
35	chr9:96082600-96083000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr9:96082600-96083200	Enhancers	Brain Germinal Matrix	brain
37	chr9:96082600-96083400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:96082600-96084000	Strong transcription	Pancreas	Pancrea
39	chr9:96082600-96086800	Weak transcription	Fetal Intestine Large	intestine
40	chr9:96082600-96088200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr9:96082800-96083000	Weak transcription	Fetal Stomach	stomach
42	chr9:96082800-96083400	Enhancers	Fetal Thymus	thymus

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