Variant report

Variant	nsv593463
Chromosome Location	chr4:3670686-3714185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:2687)
Chromatin interactive
region (count:26)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3673560-3674036	HepG2	liver:	n/a	n/a
2	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
7	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
8	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
10	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
11	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
12	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
13	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
15	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
16	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr4:3677024-3677462	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr4:3676953-3677446	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:3677080-3677230	SK-N-SH_RA	brain:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
20	CTCF	chr4:3677124-3677282	K562	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
21	CTCF	chr4:3679485-3679621	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:3677025-3677302	K562	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
23	CTCF	chr4:3679505-3679566	Gliobla	brain:	n/a	n/a
24	CTCF	chr4:3703301-3703427	MCF-7	breast:	n/a	chr4:3703375-3703384
25	CTCF	chr4:3677197-3677234	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:3679460-3679610	GM12873	blood:	n/a	n/a
27	CTCF	chr4:3676992-3677347	H1-hESC	embryonic stem cell:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
28	CTCF	chr4:3677190-3677250	ProgFib	skin:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
29	CTCF	chr4:3670560-3670710	HCT-116	colon:	n/a	n/a
30	CTCF	chr4:3677063-3677287	K562	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
31	CTCF	chr4:3703240-3703390	SK-N-SH_RA	brain:	n/a	chr4:3703375-3703384
32	CTCF	chr4:3703220-3703370	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr4:3677140-3677290	GM12864	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
34	CTCF	chr4:3677080-3677230	HCT-116	colon:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
35	CTCF	chr4:3677097-3677326	K562	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
36	CTCF	chr4:3703320-3703470	HEK293	kidney:	n/a	chr4:3703375-3703384
37	CTCF	chr4:3703324-3703414	MCF-7	breast:	n/a	chr4:3703375-3703384
38	CTCF	chr4:3679478-3679584	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:3698092-3698194	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:3707720-3707870	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:3677100-3677250	A549	lung:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
42	CTCF	chr4:3678060-3678210	WERI-Rb-1	eye:	n/a	chr4:3678107-3678115 chr4:3678102-3678115 chr4:3678100-3678118
43	CTCF	chr4:3703300-3703450	HepG2	liver:	n/a	chr4:3703375-3703384
44	CTCF	chr4:3679460-3679610	HepG2	liver:	n/a	n/a
45	CTCF	chr4:3687710-3687759	GM12892	blood:	n/a	n/a
46	CTCF	chr4:3703300-3703450	A549	lung:	n/a	chr4:3703375-3703384
47	CTCF	chr4:3677180-3677269	MCF-7	breast:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
48	CTCF	chr4:3703260-3703410	WERI-Rb-1	eye:	n/a	chr4:3703375-3703384
49	CTCF	chr4:3677009-3677377	H1-hESC	embryonic stem cell:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
50	CTCF	chr4:3703260-3703410	HepG2	liver:	n/a	chr4:3703375-3703384

(count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3690945-3690995	AG04449	skin:	fetal
2	chr4:3692375-3692425	MCF10A-Er-Src	breast:	n/a
3	chr4:3691033-3691083	HUVEC	blood vessel:	n/a
4	chr4:3690945-3690995	AG04449	skin:	fetal
5	chr4:3692375-3692425	MCF10A-Er-Src	breast:	n/a
6	chr4:3691033-3691083	HUVEC	blood vessel:	n/a
7	chr4:3692142-3692192	HRE	kidney:	n/a
8	chr4:3671067-3671117	HepG2	liver:	n/a
9	chr4:3685438-3685488	HRE	kidney:	n/a
10	chr4:3677553-3677603	NHBE	bronchial:	n/a
11	chr4:3713224-3713274	HUVEC	blood vessel:	n/a
12	chr4:3671199-3671249	AG09319	gingival:	n/a
13	chr4:3704824-3704874	ProgFib	skin:	n/a
14	chr4:3691297-3691347	HRPEpiC	eye:	n/a
15	chr4:3691397-3691447	HCPEpiC	choroid plexus:	n/a
16	chr4:3685438-3685488	AG09319	gingival:	n/a
17	chr4:3673098-3673148	H1-hESC	embryonic stem cell:	embryo
18	chr4:3681623-3681673	ovcar-3	ovarian:	n/a
19	chr4:3691397-3691447	HRPEpiC	eye:	n/a
20	chr4:3671697-3671747	HepG2	liver:	n/a
21	chr4:3671067-3671117	AG10803	skin:	n/a
22	chr4:3671503-3671553	AG04449	skin:	fetal
23	chr4:3685357-3685407	T-47D	breast:	n/a
24	chr4:3705147-3705197	GM06990	blood:	n/a
25	chr4:3691397-3691447	HRCEpiC	kidney:	n/a
26	chr4:3713287-3713337	NH-A	brain:	n/a
27	chr4:3692712-3692762	MCF10A-Er-Src	breast:	n/a
28	chr4:3691824-3691874	HRCEpiC	kidney:	n/a
29	chr4:3671380-3671430	GM12892	blood:	n/a
30	chr4:3692375-3692425	HCF	heart:	n/a
31	chr4:3691033-3691083	ovcar-3	ovarian:	n/a
32	chr4:3681759-3681809	GM12892	blood:	n/a
33	chr4:3704824-3704874	AG10803	skin:	n/a
34	chr4:3692712-3692762	HAEpiC	amniotic membrane:	n/a
35	chr4:3671199-3671249	HNPCEpiC	eye:	n/a
36	chr4:3690828-3690878	HCM	heart:	n/a
37	chr4:3689478-3689528	HCT-116	colon:	n/a
38	chr4:3680970-3681020	NHDF-neo	bronchial:	n/a
39	chr4:3682525-3682575	A549	lung:	n/a
40	chr4:3677553-3677603	PANC-1	pancreas:	n/a
41	chr4:3684756-3684806	NHBE	bronchial:	n/a
42	chr4:3691238-3691288	HepG2	liver:	n/a
43	chr4:3691033-3691083	HRPEpiC	eye:	n/a
44	chr4:3692712-3692762	SAEC	small airway:	n/a
45	chr4:3680970-3681020	NB4	blood:	n/a
46	chr4:3691297-3691347	PrEC	prostate:	n/a
47	chr4:3682627-3682677	SKMC	muscle:	n/a
48	chr4:3691238-3691288	AG10803	skin:	n/a
49	chr4:3713287-3713337	GM19239	blood:	n/a
50	chr4:3690828-3690878	SK-N-MC	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
2	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
3	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
4	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
5	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
6	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
7	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
8	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
9	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
10	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
11	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
12	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
13	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
14	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
15	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
16	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
17	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
18	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
19	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
20	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
21	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
22	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
23	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
24	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
25	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
26	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
2	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
3	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
4	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
5	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
6	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632

No data

Variant related genes	Relation type
ENSG00000250632	TF binding region
ENSG00000250632	CpG island
ENSG00000250632	chromatin interactions

Extended variants
information (count: 2128 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2128 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4916617	chr4:3670686-3670687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572399871	chr4:3670734-3670735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4916618	chr4:3670746-3670747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs116613316	chr4:3670754-3670755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576653159	chr4:3670777-3670778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545612996	chr4:3670799-3670800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368298672	chr4:3670817-3670818	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs531509945	chr4:3670828-3670829	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs76792298	chr4:3670841-3670842	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs61214126	chr4:3670842-3670843	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs114393299	chr4:3670889-3670890	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs4916619	chr4:3670893-3670894	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185359422	chr4:3670919-3670920	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs550413928	chr4:3670920-3670921	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs189039365	chr4:3670961-3670962	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs148527909	chr4:3670965-3670966	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs556015400	chr4:3670976-3670977	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs371774628	chr4:3670982-3670983	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs113084265	chr4:3670989-3670990	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs369465332	chr4:3671029-3671030	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs112431734	chr4:3671040-3671041	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs191995402	chr4:3671063-3671064	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs113040314	chr4:3671067-3671068	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs577729282	chr4:3671070-3671071	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs555341071	chr4:3671072-3671073	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs184188323	chr4:3671094-3671095	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs575831446	chr4:3671111-3671112	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs527723225	chr4:3671149-3671150	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs541801487	chr4:3671159-3671160	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs562003390	chr4:3671187-3671188	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs4916604	chr4:3671193-3671194	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs564037651	chr4:3671199-3671200	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs115636721	chr4:3671201-3671202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73795831	chr4:3671205-3671206	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs76048049	chr4:3671214-3671215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529472866	chr4:3671233-3671234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549436824	chr4:3671252-3671253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566385502	chr4:3671270-3671271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534971684	chr4:3671279-3671280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs16844751	chr4:3671289-3671290	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs571259147	chr4:3671342-3671343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537196440	chr4:3671347-3671348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188576774	chr4:3671364-3671365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374647237	chr4:3671370-3671371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73795832	chr4:3671381-3671382	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs59572368	chr4:3671397-3671398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57402651	chr4:3671398-3671399	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs201010132	chr4:3671399-3671400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577280670	chr4:3671413-3671414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577701257	chr4:3671415-3671416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3658600-3678000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:3669400-3693400	Weak transcription	Right Atrium	heart
3	chr4:3670000-3677600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:3670400-3671600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3670800-3671000	ZNF genes & repeats	Lung	lung
6	chr4:3670800-3671200	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:3670800-3674000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:3671000-3673000	Weak transcription	Lung	lung
9	chr4:3671200-3671400	Enhancers	Brain Anterior Caudate	brain
10	chr4:3671400-3672200	Weak transcription	Brain Anterior Caudate	brain
11	chr4:3671600-3672400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:3672000-3672600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:3672200-3672400	Enhancers	Brain Anterior Caudate	brain
14	chr4:3672400-3672800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:3672400-3673400	Weak transcription	Brain Anterior Caudate	brain
16	chr4:3672600-3673000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:3672800-3675600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:3673000-3674000	Enhancers	HepG2	liver
19	chr4:3673000-3674200	Enhancers	Pancreas	Pancrea
20	chr4:3673000-3674600	Enhancers	Lung	lung
21	chr4:3673200-3673800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:3673400-3673600	Enhancers	Brain Anterior Caudate	brain
23	chr4:3673400-3674000	Enhancers	A549	lung
24	chr4:3673400-3674200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:3673400-3674200	Bivalent Enhancer	Fetal Stomach	stomach
26	chr4:3673400-3674200	Enhancers	Gastric	stomach
27	chr4:3673600-3674400	Enhancers	Hela-S3	cervix
28	chr4:3674000-3674200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:3674000-3674200	Bivalent Enhancer	Left Ventricle	heart
30	chr4:3674000-3674200	Flanking Active TSS	A549	lung
31	chr4:3674000-3674200	Flanking Bivalent TSS/Enh	HepG2	liver
32	chr4:3674200-3674400	Bivalent Enhancer	HepG2	liver
33	chr4:3674200-3678800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:3674600-3674800	Weak transcription	Lung	lung
35	chr4:3674800-3676600	Enhancers	Lung	lung
36	chr4:3675600-3675800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:3675600-3676400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr4:3675600-3676600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr4:3675800-3676000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
40	chr4:3675800-3676200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:3676200-3677400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3676400-3677600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:3677000-3677400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:3677000-3677400	Enhancers	Spleen	Spleen
45	chr4:3677200-3677400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:3677200-3677400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr4:3677200-3678400	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr4:3677400-3677600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
49	chr4:3677400-3678000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:3677400-3678000	Weak transcription	Spleen	Spleen

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