Variant report

Variant	nsv1011405
Chromosome Location	chr4:3627954-3666370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:1710)
Chromatin interactive
region (count:35)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
2	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
5	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
6	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
8	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
9	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
10	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
11	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
13	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
15	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
16	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
17	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
18	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
19	CHD2	chr4:3657873-3658157	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
21	CHD2	chr4:3642375-3642459	HepG2	liver:	n/a	n/a
22	CTCF	chr4:3639120-3639270	HVMF	connective:	n/a	n/a
23	CTCF	chr4:3662465-3662619	GM19239	blood:	n/a	n/a
24	CTCF	chr4:3655800-3655950	HepG2	liver:	n/a	n/a
25	CTCF	chr4:3659600-3659750	AG04449	skin:	n/a	n/a
26	CTCF	chr4:3655971-3655982	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:3655840-3655990	K562	blood:	n/a	n/a
28	CTCF	chr4:3655977-3655985	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr4:3639569-3639577	LNCaP	prostate:	n/a	n/a
30	CTCF	chr4:3655921-3655956	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:3659600-3659750	BJ	skin:	n/a	n/a
32	CTCF	chr4:3654458-3654482	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:3655960-3655964	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr4:3647210-3647236	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:3655916-3655976	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr4:3642360-3642510	NB4	blood:	n/a	n/a
37	CTCF	chr4:3659660-3659810	NHEK	skin:	n/a	chr4:3659774-3659787
38	CTCF	chr4:3664796-3665076	GM19239	blood:	n/a	n/a
39	CTCF	chr4:3657820-3657970	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr4:3629970-3629976	K562	blood:	n/a	n/a
41	CTCF	chr4:3665109-3665234	GM19239	blood:	n/a	n/a
42	CTCF	chr4:3665292-3665362	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:3639314-3639336	K562	blood:	n/a	n/a
44	CTCF	chr4:3654457-3654499	GM12891	blood:	n/a	n/a
45	CTCF	chr4:3662513-3662587	NHEK	skin:	n/a	n/a
46	CTCF	chr4:3654482-3654564	GM19239	blood:	n/a	n/a
47	CTCF	chr4:3654475-3654577	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:3647145-3647281	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:3647171-3647273	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:3646151-3646188	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3664401-3664451	HCF	heart:	n/a
2	chr4:3664117-3664167	SKMC	muscle:	n/a
3	chr4:3664401-3664451	HCF	heart:	n/a
4	chr4:3664117-3664167	SKMC	muscle:	n/a
5	chr4:3664471-3664521	NHDF-neo	bronchial:	n/a
6	chr4:3652326-3652376	SKMC	muscle:	n/a
7	chr4:3644187-3644237	AG10803	skin:	n/a
8	chr4:3657880-3657930	SK-N-MC	brain:	n/a
9	chr4:3640481-3640531	Hela-S3	cervix:	n/a
10	chr4:3630746-3630796	SAEC	small airway:	n/a
11	chr4:3651354-3651404	HCPEpiC	choroid plexus:	n/a
12	chr4:3643475-3643525	SK-N-SH	brain:	n/a
13	chr4:3657880-3657930	PANC-1	pancreas:	n/a
14	chr4:3643770-3643820	ECC-1	luminal epithelium:	n/a
15	chr4:3664117-3664167	HRPEpiC	eye:	n/a
16	chr4:3630746-3630796	ProgFib	skin:	n/a
17	chr4:3644703-3644753	Jurkat	blood:	n/a
18	chr4:3643959-3644009	SKMC	muscle:	n/a
19	chr4:3643959-3644009	AG09319	gingival:	n/a
20	chr4:3643635-3643685	NHDF-neo	bronchial:	n/a
21	chr4:3664117-3664167	MCF-7	breast:	n/a
22	chr4:3664117-3664167	AG04449	skin:	fetal
23	chr4:3644703-3644753	AG10803	skin:	n/a
24	chr4:3642351-3642401	SAEC	small airway:	n/a
25	chr4:3664401-3664451	U87	brain:	n/a
26	chr4:3660005-3660055	IMR90	lung:	fetal
27	chr4:3643404-3643454	A549	lung:	n/a
28	chr4:3630746-3630796	SK-N-SH	brain:	n/a
29	chr4:3664240-3664290	A549	lung:	n/a
30	chr4:3657880-3657930	HEK293	kidney:	embryo
31	chr4:3630603-3630653	GM06990	blood:	n/a
32	chr4:3652433-3652483	MCF-7	breast:	n/a
33	chr4:3643770-3643820	HEEpiC	esophagus:	n/a
34	chr4:3664240-3664290	BJ	skin:	n/a
35	chr4:3643770-3643820	PFSK-1	brain:	n/a
36	chr4:3646912-3646962	HIPEpiC	eye:	n/a
37	chr4:3660005-3660055	MCF-7	breast:	n/a
38	chr4:3643770-3643820	HRPEpiC	eye:	n/a
39	chr4:3651233-3651283	AG04449	skin:	fetal
40	chr4:3652326-3652376	GM12878	blood:	n/a
41	chr4:3663974-3664024	MCF-7	breast:	n/a
42	chr4:3643404-3643454	ECC-1	luminal epithelium:	n/a
43	chr4:3657880-3657930	NHDF-neo	bronchial:	n/a
44	chr4:3630746-3630796	HCT-116	colon:	n/a
45	chr4:3651471-3651521	HAEpiC	amniotic membrane:	n/a
46	chr4:3643635-3643685	HepG2	liver:	n/a
47	chr4:3644437-3644487	CMK	blood:	n/a
48	chr4:3664117-3664167	HEEpiC	esophagus:	n/a
49	chr4:3664401-3664451	HIPEpiC	eye:	n/a
50	chr4:3643770-3643820	PrEC	prostate:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
2	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
3	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
4	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
5	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
6	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
7	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
8	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
9	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
10	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
11	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
12	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
13	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
14	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
15	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
16	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
17	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
18	chr4:3532356..3534055-chr4:3658252..3659865,2	K562	blood:
19	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
20	chr4:3531986..3534650-chr4:3657102..3659521,2	MCF-7	breast:
21	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
22	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
23	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
24	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
25	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
26	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
27	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
28	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
29	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
30	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
31	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
32	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
33	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
34	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
35	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-5	chr4:3650108-3650607	XLOC_003431
2	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2
3	lnc-LRPAP1-6	chr4:3645119-3645386	ucscGeneNc_uc003ghl_2
4	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
5	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
6	lnc-LRPAP1-6	chr4:3648128-3648206	ucscGeneNc_uc003ghl_2
7	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429

No data

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250681	CpG island
ENSG00000175920	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000250681	chromatin interactions

Extended variants
information (count: 2465 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2465 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41505245	chr4:3627954-3627955	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12645752	chr4:3627969-3627970	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62274330	chr4:3627977-3627978	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552852164	chr4:3627996-3627997	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569427283	chr4:3628008-3628009	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62274331	chr4:3628022-3628023	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76025379	chr4:3628036-3628037	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79998415	chr4:3628038-3628039	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531922074	chr4:3628052-3628053	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75943311	chr4:3628055-3628056	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77331355	chr4:3628067-3628068	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80033642	chr4:3628078-3628079	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548830283	chr4:3628084-3628085	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75214683	chr4:3628091-3628092	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568386274	chr4:3628094-3628095	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79696740	chr4:3628106-3628107	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534228062	chr4:3628110-3628111	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553737074	chr4:3628112-3628113	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73206710	chr4:3628119-3628120	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570655393	chr4:3628120-3628121	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73206712	chr4:3628131-3628132	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539541140	chr4:3628133-3628134	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558330410	chr4:3628154-3628155	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575354541	chr4:3628164-3628165	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544192122	chr4:3628186-3628187	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554820129	chr4:3628202-3628203	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4951832	chr4:3628203-3628204	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7375503	chr4:3628213-3628214	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540257849	chr4:3628225-3628226	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371998545	chr4:3628226-3628227	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7376474	chr4:3628238-3628239	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73206713	chr4:3628276-3628277	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375021076	chr4:3628284-3628285	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560181111	chr4:3628287-3628288	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532248499	chr4:3628289-3628290	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368562612	chr4:3628292-3628293	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73206715	chr4:3628298-3628299	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78511744	chr4:3628344-3628345	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74493343	chr4:3628347-3628348	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75608745	chr4:3628351-3628352	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111941436	chr4:3628365-3628366	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73081179	chr4:3628382-3628383	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563092776	chr4:3628386-3628387	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531906157	chr4:3628395-3628396	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75625513	chr4:3628418-3628419	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs548475609	chr4:3628425-3628426	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs73206716	chr4:3628428-3628429	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs78148814	chr4:3628441-3628442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs73081180	chr4:3628442-3628443	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs527971791	chr4:3628448-3628449	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3625000-3628000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chr4:3625200-3629400	ZNF genes & repeats	Fetal Brain Female	brain
3	chr4:3626000-3628000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:3627000-3632000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3627600-3628000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:3627800-3628400	Weak transcription	Fetal Brain Male	brain
7	chr4:3627800-3629600	ZNF genes & repeats	Spleen	Spleen
8	chr4:3628400-3629400	ZNF genes & repeats	Fetal Brain Male	brain
9	chr4:3629200-3629400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
10	chr4:3629200-3629400	Bivalent/Poised TSS	Fetal Heart	heart
11	chr4:3629400-3629600	Weak transcription	Fetal Brain Male	brain
12	chr4:3629400-3635800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:3629600-3630400	Enhancers	Fetal Brain Male	brain
14	chr4:3629800-3630200	Enhancers	Brain Anterior Caudate	brain
15	chr4:3630000-3631800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
16	chr4:3630200-3631800	Weak transcription	Brain Anterior Caudate	brain
17	chr4:3630600-3631600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:3631200-3634800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:3631800-3633800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:3632000-3632200	Enhancers	Brain Anterior Caudate	brain
21	chr4:3632000-3632800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3632200-3632400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:3632200-3632400	Bivalent Enhancer	Placenta	Placenta
24	chr4:3632200-3635800	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr4:3632400-3632600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:3632400-3632600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
27	chr4:3632400-3632600	Bivalent Enhancer	HepG2	liver
28	chr4:3632400-3633200	Enhancers	Fetal Intestine Large	intestine
29	chr4:3632600-3633000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:3632600-3633200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:3632600-3635800	ZNF genes & repeats	Fetal Stomach	stomach
32	chr4:3632800-3633000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:3633000-3633800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr4:3633000-3633800	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr4:3633000-3633800	Bivalent Enhancer	Placenta	Placenta
36	chr4:3633000-3633800	Bivalent Enhancer	HepG2	liver
37	chr4:3633000-3634200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:3633000-3634200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr4:3633000-3636400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:3633200-3634000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:3633200-3634200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:3633200-3634800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chr4:3633400-3633600	Bivalent Enhancer	Osteobl	bone
44	chr4:3633400-3633800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:3633400-3634000	Enhancers	Fetal Kidney	kidney
46	chr4:3633400-3634200	Enhancers	HSMM	muscle
47	chr4:3633400-3634200	Enhancers	HSMMtube	muscle
48	chr4:3633600-3633800	Flanking Active TSS	Osteobl	bone
49	chr4:3633800-3634200	Enhancers	Osteobl	bone
50	chr4:3634000-3640000	Weak transcription	Fetal Kidney	kidney

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