Variant report

Variant	nsv4062
Chromosome Location	chr3:150617445-150635166
allele	n/a
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	BATF	chr3:150630310-150630553	GM12878	blood:	n/a	chr3:150630501-150630511 chr3:150630500-150630511
2	BATF	chr3:150630257-150630676	GM12878	blood:	n/a	chr3:150630501-150630511 chr3:150630500-150630511
3	CEBPB	chr3:150621673-150621946	HepG2	liver:	n/a	chr3:150621799-150621812 chr3:150621801-150621810 chr3:150621800-150621811
4	CEBPB	chr3:150621761-150621905	K562	blood:	n/a	chr3:150621799-150621812 chr3:150621801-150621810 chr3:150621800-150621811
5	CEBPB	chr3:150621795-150621811	Hela-S3	cervix:	n/a	chr3:150621801-150621810 chr3:150621800-150621811
6	CEBPB	chr3:150621740-150621837	A549	lung:	n/a	chr3:150621799-150621812 chr3:150621801-150621810 chr3:150621800-150621811
7	CEBPB	chr3:150630052-150630450	A549	lung:	n/a	chr3:150630344-150630355 chr3:150630344-150630357 chr3:150630346-150630355 chr3:150630346-150630355 chr3:150630344-150630357 chr3:150630346-150630355 chr3:150630346-150630355
8	CTCF	chr3:150628577-150628632	GM20000	blood:	n/a	n/a
9	E2F4	chr3:150632628-150632687	MCF10A-Er-Src	breast:	n/a	n/a
10	EP300	chr3:150630629-150630630	GM12878	blood:	n/a	n/a
11	FOS	chr3:150631234-150631321	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr3:150631207-150631380	MCF10A-Er-Src	breast:	n/a	n/a
13	FOXA1	chr3:150623651-150624072	T-47D	breast:	n/a	n/a
14	FOXA1	chr3:150626895-150627253	HepG2	liver:	n/a	n/a
15	FOXA1	chr3:150623597-150623990	T-47D	breast:	n/a	n/a
16	GATA1	chr3:150620802-150621192	PBDE	blood:	n/a	chr3:150620930-150620937 chr3:150620961-150620968 chr3:150620961-150620968 chr3:150620923-150620944 chr3:150620930-150620937 chr3:150620959-150620968 chr3:150620956-150620972 chr3:150620930-150620937 chr3:150620961-150620968
17	GATA3	chr3:150623549-150624380	MCF-7	breast:	n/a	n/a
18	GATA3	chr3:150623614-150624213	T-47D	breast:	n/a	n/a
19	GATA3	chr3:150623337-150624515	MCF-7	breast:	n/a	chr3:150623406-150623413
20	GATA3	chr3:150623577-150624181	T-47D	breast:	n/a	n/a
21	GATA3	chr3:150623671-150624110	MCF-7	breast:	n/a	n/a
22	GATA3	chr3:150623636-150624226	MCF-7	breast:	n/a	n/a
23	GATA3	chr3:150621140-150621433	SH-SY5Y	brain:	n/a	n/a
24	IRF1	chr3:150621690-150621764	K562	blood:	n/a	chr3:150621713-150621725 chr3:150621713-150621725 chr3:150621708-150621725
25	JUND	chr3:150629955-150630232	HepG2	liver:	n/a	n/a
26	MAFF	chr3:150629665-150629984	HepG2	liver:	n/a	chr3:150629826-150629844
27	MAFF	chr3:150629670-150629973	K562	blood:	n/a	chr3:150629826-150629844
28	MAFK	chr3:150629682-150629994	HepG2	liver:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
29	MAFK	chr3:150629660-150630007	HepG2	liver:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
30	MAFK	chr3:150629675-150629995	K562	blood:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
31	MAFK	chr3:150629685-150629982	Hela-S3	cervix:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
32	MAFK	chr3:150626394-150626552	HepG2	liver:	n/a	n/a
33	MAFK	chr3:150626489-150626522	K562	blood:	n/a	n/a
34	MAFK	chr3:150629584-150629976	H1-hESC	embryonic stem cell:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
35	MAFK	chr3:150629650-150629988	IMR90	lung:	n/a	chr3:150629822-150629842 chr3:150629824-150629840 chr3:150629825-150629839 chr3:150629827-150629842
36	MAX	chr3:150620272-150620290	HepG2	liver:	n/a	n/a
37	MEF2A	chr3:150630320-150630684	GM12878	blood:	n/a	chr3:150630504-150630512
38	MEF2A	chr3:150630192-150630655	GM12878	blood:	n/a	chr3:150630504-150630512
39	MEF2C	chr3:150630187-150630687	GM12878	blood:	n/a	chr3:150630504-150630512
40	MYC	chr3:150625297-150625327	MCF-7	breast:	n/a	n/a
41	MYC	chr3:150633788-150633827	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr3:150625230-150625335	Gliobla	brain:	n/a	n/a
43	POLR2A	chr3:150625259-150625372	MCF-7	breast:	n/a	n/a
44	POLR2A	chr3:150619938-150619973	MCF-7	breast:	n/a	n/a
45	POLR2A	chr3:150630859-150631327	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr3:150630818-150631401	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr3:150627801-150627965	MCF-7	breast:	n/a	n/a
48	RCOR1	chr3:150631347-150631632	K562	blood:	n/a	n/a
49	RCOR1	chr3:150621795-150621931	K562	blood:	n/a	n/a
50	REST	chr3:150630656-150631555	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:150621326-150621376	ECC-1	luminal epithelium:	n/a
2	chr3:150621326-150621376	ECC-1	luminal epithelium:	n/a
3	chr3:150621326-150621376	GM12891	blood:	n/a
4	chr3:150621326-150621376	AoSMC	blood vessel:	n/a
5	chr3:150621326-150621376	HIPEpiC	eye:	n/a
6	chr3:150621326-150621376	AG04449	skin:	fetal
7	chr3:150621326-150621376	HEK293	kidney:	embryo
8	chr3:150621326-150621376	HL-60	blood:	n/a
9	chr3:150621326-150621376	GM06990	blood:	n/a
10	chr3:150621326-150621376	PrEC	prostate:	n/a
11	chr3:150621326-150621376	HNPCEpiC	eye:	n/a
12	chr3:150621326-150621376	A549	lung:	n/a
13	chr3:150621326-150621376	SAEC	small airway:	n/a
14	chr3:150621326-150621376	BE2_C	brain:	n/a
15	chr3:150621326-150621376	BJ	skin:	n/a
16	chr3:150621326-150621376	SKMC	muscle:	n/a
17	chr3:150621326-150621376	HepG2	liver:	n/a
18	chr3:150621326-150621376	T-47D	breast:	n/a
19	chr3:150621326-150621376	HCM	heart:	n/a
20	chr3:150621326-150621376	HAEpiC	amniotic membrane:	n/a
21	chr3:150621326-150621376	Hepatocyte	liver:	n/a
22	chr3:150621326-150621376	GM19239	blood:	n/a
23	chr3:150621326-150621376	Caco-2	colon:	n/a
24	chr3:150621326-150621376	AG10803	skin:	n/a
25	chr3:150621326-150621376	HRE	kidney:	n/a
26	chr3:150621326-150621376	HUVEC	blood vessel:	n/a
27	chr3:150621326-150621376	K562	blood:	n/a
28	chr3:150621326-150621376	AG09309	skin:	n/a
29	chr3:150621326-150621376	ProgFib	skin:	n/a
30	chr3:150621326-150621376	HCPEpiC	choroid plexus:	n/a
31	chr3:150621326-150621376	GM12878	blood:	n/a
32	chr3:150621326-150621376	NHBE	bronchial:	n/a
33	chr3:150621326-150621376	Jurkat	blood:	n/a
34	chr3:150621326-150621376	LNCaP	prostate:	n/a
35	chr3:150621326-150621376	MCF-7	breast:	n/a
36	chr3:150621326-150621376	PFSK-1	brain:	n/a
37	chr3:150621326-150621376	IMR90	lung:	fetal
38	chr3:150621326-150621376	SK-N-SH	brain:	n/a
39	chr3:150621326-150621376	Hela-S3	cervix:	n/a
40	chr3:150621326-150621376	HMEC	breast:	n/a
41	chr3:150621326-150621376	HCT-116	colon:	n/a
42	chr3:150621326-150621376	AG09319	gingival:	n/a
43	chr3:150621326-150621376	SK-N-MC	brain:	n/a
44	chr3:150621326-150621376	AG04450	lung:	fetal
45	chr3:150621326-150621376	H1-hESC	embryonic stem cell:	embryo
46	chr3:150621326-150621376	HCF	heart:	n/a
47	chr3:150621326-150621376	U87	brain:	n/a
48	chr3:150621326-150621376	NT2-D1	testis:	n/a
49	chr3:150621326-150621376	HEEpiC	esophagus:	n/a
50	chr3:150621326-150621376	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:150622090..150624886-chr3:150628966..150632795,3	MCF-7	breast:
2	chr3:150624732..150627491-chr3:150803111..150805628,2	MCF-7	breast:
3	chr3:150623156..150625349-chr3:150626620..150628452,2	MCF-7	breast:
4	chr3:150617220..150619793-chr3:150619915..150623246,3	MCF-7	breast:
5	chr3:150618519..150622479-chr3:150624058..150626415,3	K562	blood:
6	chr3:150622090..150624886-chr3:150628966..150632795,3	MCF-7	breast:
7	chr3:150627920..150630352-chr3:150630947..150632626,2	K562	blood:
8	chr3:150623156..150625349-chr3:150626620..150628452,2	MCF-7	breast:
9	chr3:150615182..150618213-chr3:150621326..150624872,3	K562	blood:
10	chr3:150627920..150630352-chr3:150630947..150632626,2	K562	blood:
11	chr3:150626529..150628111-chr3:150637179..150639956,2	MCF-7	breast:
12	chr3:150615265..150617813-chr3:150619650..150621718,2	MCF-7	breast:
13	chr3:150615182..150618213-chr3:150621326..150624872,3	K562	blood:
14	chr3:150614748..150616518-chr3:150617280..150620214,2	K562	blood:
15	chr3:150478330..150480784-chr3:150625078..150627756,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM188B2-1	chr3:150618941-150619243	XLOC_003285
2	lnc-FAM188B2-1	chr3:150621036-150621181	XLOC_003285

Variant related genes	Relation type
ENSG00000244382	TF binding region
ENSG00000222079	TF binding region
ENSG00000244382	CpG island
ENSG00000222079	CpG island
ENSG00000244265	chromatin interactions
ENSG00000144893	chromatin interactions
ENSG00000244382	chromatin interactions
BCL2	miRNA target sites

Extended variants
information (count: 739 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146554616	chr3:150617450-150617451	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs547641681	chr3:150617462-150617463	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140020438	chr3:150617477-150617478	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116837567	chr3:150617492-150617493	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527952126	chr3:150617510-150617511	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550748913	chr3:150617556-150617557	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552416756	chr3:150617580-150617581	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569228209	chr3:150617596-150617597	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569326967	chr3:150617598-150617599	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538303482	chr3:150617611-150617612	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555205809	chr3:150617613-150617614	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374923195	chr3:150617615-150617616	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191356332	chr3:150617631-150617632	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143546772	chr3:150617642-150617643	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554433887	chr3:150617667-150617668	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs17219034	chr3:150617682-150617683	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372353946	chr3:150617683-150617684	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554481469	chr3:150617703-150617704	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567991641	chr3:150617707-150617708	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545781933	chr3:150617709-150617710	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372477200	chr3:150617751-150617752	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116575547	chr3:150617872-150617873	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575739149	chr3:150617875-150617876	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183570780	chr3:150617948-150617949	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561567552	chr3:150617980-150617981	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146880316	chr3:150618058-150618059	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376668808	chr3:150618081-150618082	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369684108	chr3:150618160-150618161	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115207603	chr3:150618174-150618175	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188253354	chr3:150618175-150618176	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532443064	chr3:150618194-150618195	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552551518	chr3:150618210-150618211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569229745	chr3:150618240-150618241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140590717	chr3:150618264-150618265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150460402	chr3:150618295-150618296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190691799	chr3:150618299-150618300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183232897	chr3:150618403-150618404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374106658	chr3:150618432-150618433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554216351	chr3:150618460-150618461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571113979	chr3:150618474-150618475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539702695	chr3:150618478-150618479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556124523	chr3:150618488-150618489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201179818	chr3:150618518-150618519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187904494	chr3:150618530-150618531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541540030	chr3:150618536-150618537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377600222	chr3:150618553-150618554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536434376	chr3:150618554-150618555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554928726	chr3:150618559-150618560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17285010	chr3:150618575-150618576	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs564087180	chr3:150618586-150618587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	16773561	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150614400-150618200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:150614600-150618000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:150615000-150617800	Enhancers	Fetal Muscle Leg	muscle
4	chr3:150615800-150618000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr3:150616200-150618000	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:150616600-150617600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr3:150616800-150617800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:150617000-150617600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr3:150617200-150617600	Enhancers	Fetal Muscle Trunk	muscle
10	chr3:150617400-150618000	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr3:150617400-150618200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:150617400-150618200	Bivalent Enhancer	HSMMtube	muscle
13	chr3:150617600-150618400	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr3:150617800-150618200	Enhancers	Fetal Brain Female	brain
15	chr3:150617800-150619800	Weak transcription	Fetal Muscle Leg	muscle
16	chr3:150618000-150618200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:150618000-150618200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
18	chr3:150618200-150618400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:150619000-150632000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:150619800-150620600	Enhancers	Fetal Muscle Leg	muscle
21	chr3:150620400-150621400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr3:150621000-150621600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:150621000-150621600	Enhancers	HepG2	liver
24	chr3:150621400-150626400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr3:150621600-150622000	Bivalent Enhancer	Fetal Lung	lung
26	chr3:150624600-150628800	Weak transcription	Fetal Heart	heart
27	chr3:150626600-150626800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:150626800-150627000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr3:150627000-150627600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:150627400-150627600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr3:150627400-150627600	Enhancers	Fetal Intestine Large	intestine
32	chr3:150627600-150632400	Enhancers	Fetal Muscle Leg	muscle
33	chr3:150627800-150628200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr3:150628600-150632400	Enhancers	HSMMtube	muscle
35	chr3:150628800-150632400	Enhancers	Fetal Heart	heart
36	chr3:150629600-150630000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:150629600-150631400	Enhancers	Fetal Brain Male	brain
38	chr3:150629600-150631600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr3:150629600-150631600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr3:150630000-150630400	Enhancers	GM12878-XiMat	blood
41	chr3:150630400-150630600	Flanking Active TSS	GM12878-XiMat	blood
42	chr3:150630600-150631000	Enhancers	GM12878-XiMat	blood
43	chr3:150630600-150632200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr3:150630800-150631200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:150631000-150631200	Enhancers	Fetal Stomach	stomach
46	chr3:150631000-150631200	Enhancers	Psoas Muscle	Psoas
47	chr3:150631000-150631200	Flanking Active TSS	GM12878-XiMat	blood
48	chr3:150631000-150631400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr3:150631200-150632200	Enhancers	Fetal Lung	lung
50	chr3:150631400-150635000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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