Variant report

Variant	rs553156172
Chromosome Location	chr9:136398476-136398477
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	RAD21	chr9:136398098-136398603	HepG2	liver:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
2	YY1	chr9:136398169-136398481	K562	blood:	n/a	n/a
3	CTCF	chr9:136398360-136398510	GM12878	blood:	n/a	n/a
4	RAD21	chr9:136398187-136398589	HepG2	liver:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
5	RAD21	chr9:136398054-136398742	MCF-7	breast:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
6	JUN	chr9:136398048-136398635	K562	blood:	n/a	n/a
7	CTCF	chr9:136398202-136398503	K562	blood:	n/a	n/a
8	RAD21	chr9:136398166-136398615	H1-hESC	embryonic stem cell:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
9	CTCF	chr9:136398217-136398500	MCF-7	breast:	n/a	n/a
10	MAX	chr9:136398060-136398643	MCF-7	breast:	n/a	n/a
11	RUNX3	chr9:136398193-136398587	GM12878	blood:	n/a	n/a
12	CTCF	chr9:136398198-136398504	NHEK	skin:	n/a	n/a
13	RAD21	chr9:136397887-136398790	HCT-116	colon:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136397926-136397939 chr9:136398364-136398376
14	RAD21	chr9:136398134-136398582	H1-hESC	embryonic stem cell:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
15	YY1	chr9:136398160-136398532	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr9:136398209-136398498	Fibrobl	skin:	n/a	n/a
17	RAD21	chr9:136398116-136398539	HepG2	liver:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
18	CTCF	chr9:136398206-136398612	HepG2	liver:	n/a	n/a
19	CTCF	chr9:136397766-136398950	SK-N-SH	brain:	n/a	chr9:136397961-136397969
20	CTCF	chr9:136398170-136398525	K562	blood:	n/a	n/a
21	CTCF	chr9:136397936-136398797	HCT-116	colon:	n/a	chr9:136397961-136397969
22	RAD21	chr9:136398058-136398607	H1-hESC	embryonic stem cell:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
23	CTCF	chr9:136398221-136398498	LNCaP	prostate:	n/a	n/a
24	RAD21	chr9:136398197-136398548	A549	lung:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
25	CTCF	chr9:136398208-136398510	MCF-7	breast:	n/a	n/a
26	GABPA	chr9:136398085-136398540	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:136398148-136398596	K562	blood:	n/a	n/a
28	MAZ	chr9:136398188-136398536	K562	blood:	n/a	n/a
29	CTCF	chr9:136398340-136398490	HRE	kidney:	n/a	n/a
30	CTCF	chr9:136398191-136398518	GM12891	blood:	n/a	n/a
31	CTCF	chr9:136398256-136398477	GM10248	blood:	n/a	n/a
32	TCF12	chr9:136398227-136398486	GM12878	blood:	n/a	n/a
33	CTCF	chr9:136398245-136398479	Kidney_OC	kidney:	n/a	n/a
34	TCF12	chr9:136398221-136398491	H1-hESC	embryonic stem cell:	n/a	n/a
35	RAD21	chr9:136398118-136398661	ECC-1	luminal epithelium:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
36	EP300	chr9:136398190-136398508	K562	blood:	n/a	n/a
37	IRF4	chr9:136398113-136398539	GM12878	blood:	n/a	n/a
38	CTCF	chr9:136398147-136398631	K562	blood:	n/a	n/a
39	TCF12	chr9:136398027-136398546	A549	lung:	n/a	n/a
40	YY1	chr9:136398148-136398601	HepG2	liver:	n/a	n/a
41	CTCF	chr9:136398190-136398497	H1-hESC	embryonic stem cell:	n/a	n/a
42	RAD21	chr9:136398166-136398624	A549	lung:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
43	RAD21	chr9:136398172-136398558	SK-N-SH_RA	brain:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376
44	CTCF	chr9:136398168-136398553	GM12878	blood:	n/a	n/a
45	TBL1XR1	chr9:136398337-136398520	K562	blood:	n/a	n/a
46	CTCF	chr9:136398165-136398585	K562	blood:	n/a	n/a
47	CTCF	chr9:136398215-136398511	GM19240	blood:	n/a	n/a
48	CTCF	chr9:136398178-136398516	GM19238	blood:	n/a	n/a
49	CEBPB	chr9:136398222-136398559	H1-hESC	embryonic stem cell:	n/a	n/a
50	RAD21	chr9:136398200-136398579	Hela-S3	cervix:	n/a	chr9:136398364-136398374 chr9:136398362-136398375 chr9:136398364-136398376

No.	Distal block	Cell Line	Cell type
1	chr9:136397949..136398752-chr9:136594528..136595564,4	MCF-7	breast:
2	chr9:136397976..136398826-chr9:136528405..136529390,2	MCF-7	breast:
3	chr6:138026186..138027074-chr9:136397930..136398654,2	MCF-7	breast:
4	chr9:136397453..136398861-chr9:136590869..136592101,16	MCF-7	breast:
5	chr9:136391559..136394179-chr9:136396681..136398640,3	MCF-7	breast:
6	chr9:136397889..136398896-chr9:136591136..136592105,6	MCF-7	breast:
7	chr9:136397639..136398833-chr9:136580643..136581791,10	MCF-7	breast:
8	chr9:136397959..136398834-chr9:136591115..136592093,4	K562	blood:
9	chr9:136398068..136398571-chr9:136594557..136595220,2	MCF-7	breast:
10	chr9:136398236..136398863-chr9:136573868..136574473,2	MCF-7	breast:
11	chr9:136397924..136398838-chr9:136580700..136581803,6	MCF-7	breast:
12	chr9:136397854..136398745-chr9:136593068..136593594,3	K562	blood:

Variant related genes	Relation type
TMEM8C	TF binding region
ADAMTSL2	TF binding region
ENSG00000187616	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894059	chr9:136123840-136486929	Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv894077	chr9:136166346-136515297	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv894078	chr9:136194595-136484292	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
4	nsv933226	chr9:136224559-136407071	Enhancers Strong transcription Active TSS Weak 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 target site	35 gene(s)	inside rSNPs	diseases
5	nsv894081	chr9:136227260-136678954	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv894083	chr9:136281753-136452144	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv894084	chr9:136281753-136458311	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv894085	chr9:136281753-136478442	Bivalent Enhancer Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv894086	chr9:136281753-136657960	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	nsv894092	chr9:136311679-136452144	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv894093	chr9:136311679-136458311	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv894094	chr9:136311679-136528721	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
13	nsv530972	chr9:136324358-136643044	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
14	nsv894097	chr9:136333356-136407208	Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv894098	chr9:136335824-136452144	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	nsv894099	chr9:136337168-136459543	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
17	nsv894100	chr9:136371224-136547602	Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv894101	chr9:136378650-136458311	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
19	nsv894102	chr9:136388223-136496708	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	nsv894103	chr9:136397195-136442192	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
21	nsv615637	chr9:136397834-136404516	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136392200-136398800	Weak transcription	Gastric	stomach
2	chr9:136393200-136398600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:136393600-136399400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr9:136394200-136398600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:136394200-136398600	Weak transcription	Fetal Kidney	kidney
6	chr9:136394200-136399200	Weak transcription	Left Ventricle	heart
7	chr9:136394200-136399200	Weak transcription	Pancreas	Pancrea
8	chr9:136394400-136398600	Weak transcription	Ovary	ovary
9	chr9:136394400-136399200	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr9:136394600-136399200	Weak transcription	Fetal Heart	heart
11	chr9:136395000-136399000	Weak transcription	Fetal Brain Female	brain
12	chr9:136395400-136398800	Weak transcription	Right Ventricle	heart
13	chr9:136397000-136398600	Enhancers	Fetal Thymus	thymus
14	chr9:136397600-136398600	Enhancers	Primary B cells from cord blood	blood
15	chr9:136397600-136398600	Enhancers	Primary T cells from cord blood	blood
16	chr9:136397600-136398600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr9:136397600-136398800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:136397600-136398800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr9:136397600-136399200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr9:136397600-136399200	Enhancers	Primary hematopoietic stem cells	blood
21	chr9:136397600-136399200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr9:136397600-136399200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr9:136397600-136399200	Enhancers	Brain Substantia Nigra	brain
24	chr9:136397600-136399200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
25	chr9:136397800-136398600	Bivalent Enhancer	Colonic Mucosa	Colon
26	chr9:136397800-136398800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr9:136397800-136399200	Enhancers	Liver	Liver
28	chr9:136397800-136399200	Enhancers	Brain Hippocampus Middle	brain
29	chr9:136397800-136399600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr9:136397800-136399600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr9:136397800-136400400	Enhancers	HSMM	muscle
32	chr9:136398000-136399000	Enhancers	Stomach Smooth Muscle	stomach
33	chr9:136398000-136399200	Enhancers	Brain Germinal Matrix	brain
34	chr9:136398000-136399200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr9:136398000-136399200	Enhancers	Right Atrium	heart
36	chr9:136398000-136399400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:136398000-136399400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:136398000-136399600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
39	chr9:136398000-136399800	Enhancers	Brain Angular Gyrus	brain
40	chr9:136398000-136400000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:136398000-136400200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
42	chr9:136398000-136400200	Bivalent Enhancer	Placenta	Placenta
43	chr9:136398000-136400200	Enhancers	HSMMtube	muscle
44	chr9:136398200-136398600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:136398200-136398600	Weak transcription	Spleen	Spleen
46	chr9:136398200-136398800	Enhancers	Brain Anterior Caudate	brain
47	chr9:136398200-136398800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
48	chr9:136398200-136399200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:136398200-136399200	Enhancers	Brain Cingulate Gyrus	brain
50	chr9:136398200-136399400	Bivalent Enhancer	Thymus	Thymus

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