Variant report

Variant	rs35925646
Chromosome Location	chr4:663630-663631
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:662898-665821	MCF10A-Er-Src	breast:	n/a	n/a
2	NFATC1	chr4:663535-663963	GM12878	blood:	n/a	n/a
3	POLR2A	chr4:663303-663771	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr4:663555-664005	SK-N-MC	brain:	n/a	n/a
5	POLR2A	chr4:663581-663860	HepG2	liver:	n/a	n/a
6	POLR2A	chr4:663500-664113	HL-60	blood:	n/a	n/a
7	POLR2A	chr4:661929-664004	GM12891	blood:	n/a	n/a
8	POLR2A	chr4:662117-664008	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr4:662195-663795	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr4:662084-663976	GM12878	blood:	n/a	n/a
11	POLR2A	chr4:662127-663941	H1-hESC	embryonic stem cell:	n/a	n/a
12	FOSL2	chr4:662988-663635	HepG2	liver:	n/a	n/a
13	FOXA1	chr4:663547-663692	T-47D	breast:	n/a	n/a
14	POLR2A	chr4:662172-664005	GM12892	blood:	n/a	n/a
15	POLR2A	chr4:663495-664064	K562	blood:	n/a	n/a
16	POLR2A	chr4:663505-664061	K562	blood:	n/a	n/a
17	POLR2A	chr4:663591-663957	HepG2	liver:	n/a	n/a
18	POLR2A	chr4:662975-664089	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr4:663539-663922	K562	blood:	n/a	n/a
20	POLR2A	chr4:662239-663637	GM12878	blood:	n/a	n/a
21	POLR2A	chr4:663565-663962	Raji	blood:	n/a	n/a
22	POLR2A	chr4:662029-663984	GM12891	blood:	n/a	n/a
23	CHD2	chr4:663597-663787	K562	blood:	n/a	n/a
24	POLR2A	chr4:663585-664006	U87	brain:	n/a	n/a
25	POLR2A	chr4:663436-665182	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr4:663575-664004	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr4:663391-663815	PANC-1	pancreas:	n/a	n/a
28	POLR2A	chr4:662960-663996	MCF-7	breast:	n/a	n/a
29	POLR2A	chr4:663493-664038	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr4:663523-663953	HL-60	blood:	n/a	n/a
31	POLR2A	chr4:662018-664011	GM12892	blood:	n/a	n/a
32	POLR2A	chr4:662146-663969	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr4:662051-663649	GM12891	blood:	n/a	n/a
34	POU2F2	chr4:662380-663729	GM12891	blood:	n/a	n/a
35	POLR2A	chr4:662026-664021	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:662135-663863	GM12891	blood:	n/a	n/a
37	POLR2A	chr4:662085-663984	GM12892	blood:	n/a	n/a
38	POLR2A	chr4:662117-664071	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:663370-666542	K562	blood:	n/a	n/a
40	POLR2A	chr4:662911-664023	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:663113-666359	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr4:663549-664132	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr4:663579-663983	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr4:663564-663946	PBDE	blood:	n/a	n/a
45	POLR2A	chr4:663274-664108	PFSK-1	brain:	n/a	n/a
46	IRF4	chr4:663125-663639	GM12878	blood:	n/a	n/a
47	POLR2A	chr4:662079-663958	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:663607-664000	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:663210-666145	HepG2	liver:	n/a	n/a
50	POU2F2	chr4:662078-663739	GM12891	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:663475..665943-chr8:145718684..145721269,2	MCF-7	breast:
2	chr4:662349..665374-chr4:675709..679343,3	MCF-7	breast:
3	chr4:627338..629172-chr4:662112..664476,2	MCF-7	breast:
4	chr4:642255..644273-chr4:662905..665187,2	K562	blood:
5	chr4:606087..607621-chr4:663295..666195,2	MCF-7	breast:
6	chr4:494928..497132-chr4:662075..663676,2	K562	blood:
7	chr4:640175..641727-chr4:663332..665885,2	K562	blood:
8	chr4:608874..610845-chr4:663421..664979,2	K562	blood:

No data

Variant related genes	Relation type
MYL5	TF binding region
ENSG00000169026	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10015198	0.87[EUR][1000 genomes]
rs13101691	0.87[EUR][1000 genomes]
rs13103955	0.87[EUR][1000 genomes]
rs13104878	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13107526	0.87[EUR][1000 genomes]
rs13110755	1.00[EUR][1000 genomes]
rs13111179	0.87[EUR][1000 genomes]
rs13114299	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13116523	0.87[EUR][1000 genomes]
rs13117283	0.87[EUR][1000 genomes]
rs13118033	0.80[EUR][1000 genomes]
rs13127213	0.84[EUR][1000 genomes]
rs13133935	0.87[EUR][1000 genomes]
rs13136626	0.87[EUR][1000 genomes]
rs13139052	0.84[EUR][1000 genomes]
rs13139089	0.87[EUR][1000 genomes]
rs13143415	0.95[EUR][1000 genomes]
rs13147797	0.87[EUR][1000 genomes]
rs13150119	0.87[EUR][1000 genomes]
rs28654405	0.87[EUR][1000 genomes]
rs28687729	0.87[EUR][1000 genomes]
rs28754934	0.87[EUR][1000 genomes]
rs34053163	0.87[EUR][1000 genomes]
rs34075612	0.87[EUR][1000 genomes]
rs34094325	0.87[EUR][1000 genomes]
rs34096984	0.87[EUR][1000 genomes]
rs34165278	0.87[EUR][1000 genomes]
rs34293668	0.87[EUR][1000 genomes]
rs34363025	0.87[EUR][1000 genomes]
rs34366493	0.87[EUR][1000 genomes]
rs34391278	0.87[EUR][1000 genomes]
rs34402770	0.87[EUR][1000 genomes]
rs34421911	0.87[EUR][1000 genomes]
rs34477049	0.87[EUR][1000 genomes]
rs34568772	0.87[EUR][1000 genomes]
rs34585712	0.87[EUR][1000 genomes]
rs34587191	0.84[EUR][1000 genomes]
rs34698095	0.87[EUR][1000 genomes]
rs34953355	0.87[EUR][1000 genomes]
rs34992186	0.87[EUR][1000 genomes]
rs35006826	0.87[EUR][1000 genomes]
rs35137658	0.87[EUR][1000 genomes]
rs35158410	0.87[EUR][1000 genomes]
rs35207129	0.87[EUR][1000 genomes]
rs35219160	0.87[EUR][1000 genomes]
rs35270524	0.87[EUR][1000 genomes]
rs35455427	0.87[EUR][1000 genomes]
rs35535457	0.87[EUR][1000 genomes]
rs35564967	0.87[EUR][1000 genomes]
rs35621318	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35621580	0.87[EUR][1000 genomes]
rs35649145	0.87[EUR][1000 genomes]
rs35694609	0.87[EUR][1000 genomes]
rs35732782	0.87[EUR][1000 genomes]
rs35843044	0.87[EUR][1000 genomes]
rs35853545	0.87[EUR][1000 genomes]
rs35869797	0.87[EUR][1000 genomes]
rs35894204	0.87[EUR][1000 genomes]
rs35896648	0.87[EUR][1000 genomes]
rs35935310	0.87[EUR][1000 genomes]
rs35972513	0.87[EUR][1000 genomes]
rs36060793	0.87[EUR][1000 genomes]
rs36117387	0.87[EUR][1000 genomes]
rs61760239	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71602477	0.87[EUR][1000 genomes]
rs71602479	0.87[EUR][1000 genomes]
rs71602480	0.87[EUR][1000 genomes]
rs71602481	0.87[EUR][1000 genomes]
rs71602482	0.87[EUR][1000 genomes]
rs71602484	0.87[EUR][1000 genomes]
rs71602486	0.87[EUR][1000 genomes]
rs71602489	0.87[EUR][1000 genomes]
rs71602492	0.87[EUR][1000 genomes]
rs71602500	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71602501	0.81[EUR][1000 genomes]
rs7672426	0.87[EUR][1000 genomes]
rs7685281	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
9	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
14	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers 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	22 gene(s)	inside rSNPs	diseases
15	nsv878248	chr4:645300-685993	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	nsv878249	chr4:649639-691026	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
17	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
18	esv3380332	chr4:661052-664650	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
19	esv3500540	chr4:661848-664051	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
20	esv3466955	chr4:662412-663705	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
21	esv3466956	chr4:662412-663705	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
22	nsv511246	chr4:662451-663908	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	esv3349778	chr4:662992-663664	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	esv3384754	chr4:663071-663750	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	esv3500542	chr4:663122-663689	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
26	esv3500543	chr4:663122-663689	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:658000-664400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:658000-667000	Weak transcription	Small Intestine	intestine
3	chr4:658000-667400	Weak transcription	Aorta	Aorta
4	chr4:658200-664400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:658200-664400	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:658200-664400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr4:658200-664400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:658200-664600	Weak transcription	Pancreas	Pancrea
9	chr4:658200-664600	Weak transcription	HUVEC	blood vessel
10	chr4:658200-664800	Weak transcription	Gastric	stomach
11	chr4:658200-665000	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:658200-666800	Weak transcription	Right Atrium	heart
13	chr4:658200-667000	Weak transcription	Stomach Mucosa	stomach
14	chr4:658200-667200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:658400-663800	Weak transcription	Primary T cells from cord blood	blood
16	chr4:658400-663800	Weak transcription	Brain Germinal Matrix	brain
17	chr4:658400-664400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:658400-664400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr4:658400-664400	Weak transcription	Liver	Liver
20	chr4:658400-664400	Weak transcription	Left Ventricle	heart
21	chr4:658400-664400	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr4:658400-664400	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr4:658400-664400	Weak transcription	Rectal Smooth Muscle	rectum
24	chr4:658400-664400	Weak transcription	HMEC	breast
25	chr4:658400-664600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:658400-664600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr4:658400-664600	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr4:658400-664600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:658400-664600	Weak transcription	Fetal Brain Female	brain
30	chr4:658400-664600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:658400-664600	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr4:658400-664600	Weak transcription	NH-A	brain
33	chr4:658400-664800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:658400-665000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr4:658400-665000	Weak transcription	Fetal Lung	lung
36	chr4:658400-665200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:658400-665200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr4:658400-665200	Weak transcription	Right Ventricle	heart
39	chr4:658400-665400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr4:658400-665400	Weak transcription	Fetal Kidney	kidney
41	chr4:658400-667000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr4:658600-664400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr4:658600-667000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:658600-667000	Weak transcription	Fetal Brain Male	brain
45	chr4:658800-664200	Weak transcription	Thymus	Thymus
46	chr4:658800-664400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:658800-664400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr4:658800-664400	Weak transcription	Fetal Thymus	thymus
49	chr4:658800-664600	Weak transcription	Lung	lung
50	chr4:658800-665400	Weak transcription	GM12878-XiMat	blood

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