Variant report

Variant	rs753697
Chromosome Location	chr9:96053617-96053618
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:96053072-96053780	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr9:96053372-96053896	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:95895371..95897569-chr9:96051553..96053776,2	MCF-7	breast:
2	chr9:96050880..96053674-chr9:96053740..96056815,3	MCF-7	breast:
3	chr9:96052036..96053904-chr9:96213683..96215917,2	K562	blood:

Variant related genes	Relation type
WNK2	TF binding region
ENSG00000188938	Chromatin interaction
ENSG00000048828	Chromatin interaction
ENSG00000165238	Chromatin interaction
ENSG00000131669	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12348559	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12553462	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12554962	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17594889	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34610897	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs41308906	0.90[EUR][1000 genomes]
rs4743910	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4743912	0.89[EUR][1000 genomes]
rs4744191	1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.98[ASN][1000 genomes]
rs4744193	0.98[ASN][1000 genomes]
rs4744194	0.86[CEU][hapmap]
rs4744198	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4744199	1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.81[TSI][hapmap];0.95[ASN][1000 genomes]
rs4744216	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744232	0.92[CEU][hapmap]
rs59616569	0.90[EUR][1000 genomes]
rs60604890	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73512403	0.80[EUR][1000 genomes]
rs73523697	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73527611	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73527643	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73527659	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7864826	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[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:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96027200-96056000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr9:96027200-96061000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:96031400-96054600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:96031400-96055000	Weak transcription	Colonic Mucosa	Colon
5	chr9:96031400-96062800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:96033000-96054600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:96033000-96055000	Weak transcription	Brain Anterior Caudate	brain
8	chr9:96033000-96067200	Weak transcription	Brain Angular Gyrus	brain
9	chr9:96033400-96062800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr9:96033400-96067000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr9:96033400-96077200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr9:96033600-96054600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:96033600-96060200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr9:96033600-96061000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr9:96033600-96072800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:96033800-96054600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr9:96033800-96060400	Weak transcription	Colon Smooth Muscle	Colon
18	chr9:96041600-96056800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr9:96041800-96054600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr9:96047200-96065000	Weak transcription	Fetal Brain Male	brain
21	chr9:96048200-96054600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr9:96048200-96057200	Weak transcription	Right Atrium	heart
23	chr9:96049000-96054600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr9:96049200-96057600	Strong transcription	Fetal Brain Female	brain
25	chr9:96049400-96057000	Strong transcription	Brain Germinal Matrix	brain
26	chr9:96049600-96054800	Enhancers	Fetal Thymus	thymus
27	chr9:96050000-96056600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr9:96050200-96056800	Strong transcription	Fetal Intestine Small	intestine
29	chr9:96051000-96056600	Weak transcription	Left Ventricle	heart
30	chr9:96051200-96056200	Weak transcription	Fetal Heart	heart
31	chr9:96051400-96054200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:96051400-96056400	Weak transcription	Spleen	Spleen
33	chr9:96051400-96067800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr9:96051800-96055600	Strong transcription	Pancreas	Pancrea
35	chr9:96052000-96054000	Weak transcription	Right Ventricle	heart
36	chr9:96052000-96054400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:96052000-96056800	Strong transcription	Fetal Intestine Large	intestine
38	chr9:96052000-96060800	Weak transcription	Placenta	Placenta
39	chr9:96052200-96054600	Weak transcription	Gastric	stomach
40	chr9:96052200-96056600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:96052200-96066600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:96052400-96057400	Strong transcription	Stomach Smooth Muscle	stomach
43	chr9:96052800-96054600	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr9:96052800-96056200	Weak transcription	HepG2	liver
45	chr9:96053600-96054600	Weak transcription	Fetal Stomach	stomach

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