Variant report

Variant	rs73295697
Chromosome Location	chr17:17677852-17677853
allele	A/G
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	NR3C1	chr17:17677370-17678029	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
2	RAD21	chr17:17677773-17678343	H1-hESC	embryonic stem cell:	n/a	n/a
3	RAD21	chr17:17677706-17678366	HCT-116	colon:	n/a	chr17:17677758-17677771
4	STAT3	chr17:17677281-17678154	MCF10A-Er-Src	breast:	n/a	chr17:17677423-17677434
5	RAD21	chr17:17677835-17678207	MCF-7	breast:	n/a	n/a
6	TCF12	chr17:17677802-17678354	A549	lung:	n/a	chr17:17677967-17677974
7	FOS	chr17:17677302-17678029	MCF10A-Er-Src	breast:	n/a	n/a
8	RAD21	chr17:17677844-17678218	H1-hESC	embryonic stem cell:	n/a	n/a
9	MYC	chr17:17677041-17678162	MCF10A-Er-Src	breast:	n/a	chr17:17677060-17677070 chr17:17677295-17677304
10	POLR2A	chr17:17677846-17677859	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr17:17677293-17678519	A549	lung:	n/a	n/a
12	STAT3	chr17:17677834-17678034	MCF10A-Er-Src	breast:	n/a	n/a
13	STAT3	chr17:17677263-17678154	MCF10A-Er-Src	breast:	n/a	chr17:17677423-17677434
14	NR3C1	chr17:17677476-17677999	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
15	POLR2A	chr17:17677365-17677940	MCF10A-Er-Src	breast:	n/a	n/a
16	RAD21	chr17:17677817-17678255	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr17:17677720-17677870	NHEK	skin:	n/a	n/a
18	NR3C1	chr17:17677392-17677986	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
19	RAD21	chr17:17677536-17678419	SK-N-SH	brain:	n/a	chr17:17677758-17677771
20	MYC	chr17:17677240-17678157	MCF10A-Er-Src	breast:	n/a	chr17:17677295-17677304
21	MAX	chr17:17677267-17678328	A549	lung:	n/a	chr17:17677295-17677304
22	FOS	chr17:17677303-17678132	MCF10A-Er-Src	breast:	n/a	n/a
23	CREB1	chr17:17677425-17678030	A549	lung:	n/a	n/a
24	NR3C1	chr17:17677338-17678145	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
25	POLR2A	chr17:17677551-17678055	MCF10A-Er-Src	breast:	n/a	n/a
26	CTCF	chr17:17677767-17678429	SK-N-SH	brain:	n/a	n/a
27	RAD21	chr17:17677730-17678379	A549	lung:	n/a	chr17:17677758-17677771
28	NR3C1	chr17:17677267-17678186	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
29	RAD21	chr17:17677819-17678346	A549	lung:	n/a	n/a
30	NR3C1	chr17:17677333-17678146	A549	lung:	n/a	chr17:17677654-17677663 chr17:17677865-17677878 chr17:17677867-17677882
31	RAD21	chr17:17677849-17678178	SK-N-SH_RA	brain:	n/a	n/a
32	FOS	chr17:17677320-17678140	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17668920..17670836-chr17:17676524..17679052,2	MCF-7	breast:
2	chr17:17584533..17585363-chr17:17677613..17678120,2	MCF-7	breast:
3	chr17:17662991..17666589-chr17:17675062..17678538,4	MCF-7	breast:
4	chr17:17662619..17665497-chr17:17675945..17678839,3	K562	blood:
5	chr17:17676883..17678568-chr17:17694374..17695879,2	MCF-7	breast:
6	chr17:17675195..17678001-chr17:17679106..17680835,2	MCF-7	breast:
7	chr17:17612942..17614655-chr17:17676717..17679222,2	MCF-7	breast:
8	chr17:17654401..17657547-chr17:17674732..17678193,3	K562	blood:
9	chr17:17583496..17585478-chr17:17676314..17678028,2	MCF-7	breast:
10	chr17:17676793..17678855-chr17:17691201..17693864,2	MCF-7	breast:

Variant related genes	Relation type
RAI1-AS1	TF binding region
ENSG00000264167	TF binding region
ENSG00000108557	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11078396	1.00[ASN][1000 genomes]
rs12103565	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12600386	1.00[EUR][1000 genomes]
rs12601751	1.00[EUR][1000 genomes]
rs12603026	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12603069	1.00[EUR][1000 genomes]
rs12603397	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58667361	1.00[EUR][1000 genomes]
rs73300562	1.00[EUR][1000 genomes]
rs9910075	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
6	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
8	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv833385	chr17:17594037-17765578	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
11	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv543241	chr17:17596222-17703059	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1062361	chr17:17598407-17746899	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
17	nsv543243	chr17:17598407-17746899	Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
18	nsv907756	chr17:17619859-17747289	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
19	nsv522668	chr17:17619859-17752809	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
20	nsv907757	chr17:17619859-17752809	Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
21	nsv907758	chr17:17619859-17782404	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
22	nsv907759	chr17:17619859-17802478	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	nsv532109	chr17:17630064-17700497	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv1059949	chr17:17632590-17803194	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
25	nsv543244	chr17:17632590-17803194	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
26	nsv907760	chr17:17649423-17782404	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
27	nsv907761	chr17:17649423-17802478	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
28	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
29	nsv907762	chr17:17668071-17802478	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
30	esv1804029	chr17:17669662-17714250	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
31	nsv907763	chr17:17673824-17749822	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
32	nsv907764	chr17:17673824-17754633	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17656600-17682200	Weak transcription	Small Intestine	intestine
2	chr17:17662000-17683800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr17:17666400-17681800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr17:17668600-17678200	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr17:17669000-17678400	Enhancers	Colon Smooth Muscle	Colon
6	chr17:17669400-17678600	Enhancers	Fetal Muscle Leg	muscle
7	chr17:17669800-17678200	Enhancers	Right Ventricle	heart
8	chr17:17669800-17682600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr17:17670000-17680400	Weak transcription	Dnd41	blood
10	chr17:17670200-17680800	Weak transcription	Primary T cells from cord blood	blood
11	chr17:17670200-17683000	Weak transcription	Thymus	Thymus
12	chr17:17670400-17681600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr17:17670600-17679600	Enhancers	Fetal Muscle Trunk	muscle
14	chr17:17670800-17682000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr17:17671000-17683600	Weak transcription	Liver	Liver
16	chr17:17671400-17681200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr17:17671400-17684400	Weak transcription	Primary B cells from cord blood	blood
18	chr17:17671600-17679400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr17:17672600-17681400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr17:17673000-17681200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr17:17673200-17681200	Weak transcription	Fetal Thymus	thymus
22	chr17:17673400-17681000	Weak transcription	HepG2	liver
23	chr17:17673800-17681000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr17:17674600-17680600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr17:17674600-17681800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr17:17674800-17678400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr17:17674800-17681800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:17674800-17683600	Weak transcription	Fetal Brain Male	brain
29	chr17:17675000-17683800	Weak transcription	Fetal Brain Female	brain
30	chr17:17675200-17678400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr17:17675200-17678400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr17:17675200-17681800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr17:17675400-17681000	Weak transcription	Ovary	ovary
34	chr17:17675600-17681400	Weak transcription	NHLF	lung
35	chr17:17675800-17681200	Weak transcription	Adipose Nuclei	Adipose
36	chr17:17675800-17681800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr17:17675800-17683800	Weak transcription	GM12878-XiMat	blood
38	chr17:17675800-17684200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr17:17676200-17679200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:17676200-17680800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr17:17676200-17683600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:17676400-17681600	Weak transcription	NHDF-Ad	bronchial
43	chr17:17676600-17678000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr17:17676600-17678000	Enhancers	A549	lung
45	chr17:17676600-17678200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr17:17676600-17678200	Enhancers	Hela-S3	cervix
47	chr17:17676600-17678200	Enhancers	NH-A	brain
48	chr17:17676600-17678400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr17:17676600-17679000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr17:17676800-17678000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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