Variant report

Variant	nsv1010726
Chromosome Location	chr3:155476547-155492177
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	BACH1	chr3:155487617-155487877	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr3:155487792-155488163	K562	blood:	n/a	n/a
3	CEBPB	chr3:155481693-155482017	A549	lung:	n/a	n/a
4	CEBPB	chr3:155481680-155482057	K562	blood:	n/a	n/a
5	CEBPB	chr3:155481678-155482001	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:155481686-155482016	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:155477996-155478082	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:155484031-155484340	K562	blood:	n/a	n/a
9	CEBPB	chr3:155484017-155484279	K562	blood:	n/a	n/a
10	CEBPB	chr3:155481714-155482101	A549	lung:	n/a	n/a
11	CEBPB	chr3:155481705-155482029	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:155477873-155478193	K562	blood:	n/a	n/a
13	CEBPB	chr3:155487739-155488080	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr3:155484008-155484489	Hela-S3	cervix:	n/a	chr3:155484369-155484386
15	CEBPB	chr3:155484002-155484366	A549	lung:	n/a	n/a
16	CEBPB	chr3:155487735-155487999	K562	blood:	n/a	n/a
17	CEBPB	chr3:155483987-155484490	IMR90	lung:	n/a	chr3:155484369-155484386
18	CEBPB	chr3:155477961-155478093	A549	lung:	n/a	n/a
19	CEBPB	chr3:155483934-155484389	MCF-7	breast:	n/a	chr3:155484369-155484386
20	CEBPB	chr3:155477835-155478185	K562	blood:	n/a	n/a
21	CTCF	chr3:155487720-155487870	GM12875	blood:	n/a	n/a
22	FOS	chr3:155483934-155484477	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
23	FOS	chr3:155483930-155484451	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
24	FOS	chr3:155484040-155484309	HUVEC	blood vessel:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
25	FOS	chr3:155483956-155484408	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
26	FOS	chr3:155483951-155484366	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
27	FOSL2	chr3:155483979-155484315	A549	lung:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
28	FOSL2	chr3:155484053-155484254	A549	lung:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
29	FOSL2	chr3:155484008-155484407	MCF-7	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
30	JUN	chr3:155484040-155484388	HepG2	liver:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
31	JUND	chr3:155483864-155484516	SK-N-SH	brain:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
32	JUND	chr3:155484016-155484379	HepG2	liver:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
33	JUND	chr3:155484017-155484384	Hela-S3	cervix:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
34	KAP1	chr3:155487787-155488193	HEK293	kidney:	n/a	n/a
35	KAP1	chr3:155487841-155488191	K562	blood:	n/a	n/a
36	MAFK	chr3:155487661-155487892	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr3:155484039-155484148	A549	lung:	n/a	n/a
38	MXI1	chr3:155492134-155492147	H1-hESC	embryonic stem cell:	n/a	n/a
39	MYC	chr3:155483937-155484362	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484199 chr3:155484189-155484198
40	MYC	chr3:155488776-155488807	MCF-7	breast:	n/a	n/a
41	MYC	chr3:155484018-155484263	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484199 chr3:155484189-155484198
42	NFYB	chr3:155484018-155484218	GM12878	blood:	n/a	chr3:155484146-155484156
43	POLR2A	chr3:155480024-155480225	K562	blood:	n/a	n/a
44	POLR2A	chr3:155481441-155481641	K562	blood:	n/a	n/a
45	POLR2A	chr3:155487952-155488156	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr3:155489099-155489186	Gliobla	brain:	n/a	n/a
47	POLR2A	chr3:155476624-155477069	K562	blood:	n/a	n/a
48	POLR2A	chr3:155488868-155489008	MCF-7	breast:	n/a	n/a
49	POLR2A	chr3:155488474-155488995	HepG2	liver:	n/a	n/a
50	POLR2A	chr3:155487935-155487947	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155480645-155480695	BJ	skin:	n/a
2	chr3:155480645-155480695	H1-hESC	embryonic stem cell:	embryo
3	chr3:155480645-155480695	RPTEC	kidney:	n/a
4	chr3:155480645-155480695	NH-A	brain:	n/a
5	chr3:155480645-155480695	Jurkat	blood:	n/a
6	chr3:155480645-155480695	SK-N-MC	brain:	n/a
7	chr3:155480645-155480695	ovcar-3	ovarian:	n/a
8	chr3:155480645-155480695	PFSK-1	brain:	n/a
9	chr3:155480645-155480695	GM19239	blood:	n/a
10	chr3:155480645-155480695	MCF10A-Er-Src	breast:	n/a
11	chr3:155480645-155480695	AG04450	lung:	fetal
12	chr3:155480645-155480695	NT2-D1	testis:	n/a
13	chr3:155480645-155480695	BE2_C	brain:	n/a
14	chr3:155480645-155480695	HCPEpiC	choroid plexus:	n/a
15	chr3:155480645-155480695	LNCaP	prostate:	n/a
16	chr3:155480645-155480695	CMK	blood:	n/a
17	chr3:155480645-155480695	SKMC	muscle:	n/a
18	chr3:155480645-155480695	SAEC	small airway:	n/a
19	chr3:155480645-155480695	HCM	heart:	n/a
20	chr3:155480645-155480695	AG04449	skin:	fetal
21	chr3:155480645-155480695	K562	blood:	n/a
22	chr3:155480645-155480695	Hepatocyte	liver:	n/a
23	chr3:155480645-155480695	HRE	kidney:	n/a
24	chr3:155480645-155480695	HAEpiC	amniotic membrane:	n/a
25	chr3:155480645-155480695	SK-N-SH_RA	brain:	n/a
26	chr3:155480645-155480695	GM12891	blood:	n/a
27	chr3:155480645-155480695	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:155480645-155480695	ProgFib	skin:	n/a
29	chr3:155480645-155480695	HEEpiC	esophagus:	n/a
30	chr3:155480645-155480695	IMR90	lung:	fetal
31	chr3:155480645-155480695	HRCEpiC	kidney:	n/a
32	chr3:155480645-155480695	HMEC	breast:	n/a
33	chr3:155480645-155480695	AG10803	skin:	n/a
34	chr3:155480645-155480695	NHDF-neo	bronchial:	n/a
35	chr3:155480645-155480695	HEK293	kidney:	embryo
36	chr3:155480645-155480695	Hela-S3	cervix:	n/a
37	chr3:155480645-155480695	GM12878	blood:	n/a
38	chr3:155480645-155480695	HNPCEpiC	eye:	n/a
39	chr3:155480645-155480695	HCF	heart:	n/a
40	chr3:155480645-155480695	HUVEC	blood vessel:	n/a
41	chr3:155480645-155480695	PrEC	prostate:	n/a
42	chr3:155480645-155480695	T-47D	breast:	n/a
43	chr3:155480645-155480695	HRPEpiC	eye:	n/a
44	chr3:155480645-155480695	SK-N-SH	brain:	n/a
45	chr3:155480645-155480695	AG09319	gingival:	n/a
46	chr3:155480645-155480695	NHBE	bronchial:	n/a
47	chr3:155480645-155480695	GM06990	blood:	n/a
48	chr3:155480645-155480695	AG09309	skin:	n/a
49	chr3:155480645-155480695	HL-60	blood:	n/a
50	chr3:155480645-155480695	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:155481429..155485286-chr3:155486373..155491702,5	K562	blood:
2	chr3:155488449..155490862-chr3:155570678..155572291,2	MCF-7	breast:
3	chr3:155480147..155483683-chr3:155487368..155490043,3	K562	blood:
4	chr3:155481429..155485286-chr3:155486373..155491702,5	K562	blood:
5	chr3:155479593..155481988-chr3:155483221..155485642,3	K562	blood:
6	chr3:155483233..155486124-chr3:155587848..155589390,2	MCF-7	breast:
7	chr3:155491831..155494360-chr3:155588180..155590433,3	K562	blood:
8	chr3:155491839..155493601-chr3:155495108..155496890,2	K562	blood:
9	chr3:155468097..155470070-chr3:155473602..155476572,2	K562	blood:
10	chr3:155476567..155478417-chr3:155522248..155524245,2	MCF-7	breast:
11	chr3:155489353..155491545-chr3:155498387..155500105,2	MCF-7	breast:
12	chr3:155371134..155373846-chr3:155480180..155482982,2	K562	blood:
13	chr3:155479593..155481988-chr3:155483221..155485642,3	K562	blood:
14	chr3:155477418..155480054-chr3:155586699..155588871,2	MCF-7	breast:
15	chr3:155489809..155491892-chr3:155496902..155499266,2	K562	blood:
16	chr3:155480147..155483683-chr3:155487368..155490043,3	K562	blood:
17	chr3:155475971..155478376-chr3:155587732..155590081,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GMPS-3	chr3:155478406-155479006	NONHSAT092842

Variant related genes	Relation type
ENSG00000241307	TF binding region
ENSG00000241307	CpG island
ENSG00000174928	chromatin interactions
ENSG00000163655	chromatin interactions
ENSG00000169359	chromatin interactions

Extended variants
information (count: 594 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7621415	chr3:155476547-155476548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180888409	chr3:155476597-155476598	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148900945	chr3:155476605-155476606	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143471364	chr3:155476629-155476630	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs546185612	chr3:155476656-155476657	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs558380824	chr3:155476657-155476658	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs573455182	chr3:155476717-155476718	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs540662550	chr3:155476742-155476743	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs112602885	chr3:155476774-155476775	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs529373978	chr3:155476783-155476784	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs139220370	chr3:155476902-155476903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs137881965	chr3:155476961-155476962	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs563153909	chr3:155476986-155476987	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs185964168	chr3:155476987-155476988	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs115231899	chr3:155477020-155477021	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs564448495	chr3:155477029-155477030	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs6441012	chr3:155477033-155477034	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142098748	chr3:155477123-155477124	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs145888464	chr3:155477180-155477181	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138706717	chr3:155477183-155477184	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs9877489	chr3:155477191-155477192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs57183957	chr3:155477201-155477202	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150866362	chr3:155477202-155477203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540072064	chr3:155477207-155477208	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190865989	chr3:155477208-155477209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138348498	chr3:155477233-155477234	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs112947781	chr3:155477234-155477235	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs183443773	chr3:155477242-155477243	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144253286	chr3:155477257-155477258	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140033561	chr3:155477264-155477265	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143561024	chr3:155477303-155477304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs578029211	chr3:155477312-155477313	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs76970216	chr3:155477313-155477314	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs80255281	chr3:155477323-155477324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs564106276	chr3:155477347-155477348	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543302241	chr3:155477380-155477381	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528411212	chr3:155477451-155477452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs111959466	chr3:155477488-155477489	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561674861	chr3:155477492-155477493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187420137	chr3:155477493-155477494	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146334674	chr3:155477507-155477508	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569014077	chr3:155477514-155477515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190538645	chr3:155477547-155477548	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551977550	chr3:155477592-155477593	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367917970	chr3:155477596-155477597	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183144985	chr3:155477664-155477665	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534518604	chr3:155477689-155477690	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139578929	chr3:155477726-155477727	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78947157	chr3:155477770-155477771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376994174	chr3:155477856-155477857	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155463800-155487800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:155463800-155501200	Weak transcription	Aorta	Aorta
3	chr3:155464000-155476600	Weak transcription	Ovary	ovary
4	chr3:155464200-155487600	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:155464200-155487600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:155464200-155487800	Weak transcription	Adipose Nuclei	Adipose
7	chr3:155464200-155487800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:155464200-155487800	Weak transcription	Pancreas	Pancrea
9	chr3:155464200-155489600	Weak transcription	Brain Anterior Caudate	brain
10	chr3:155464200-155490600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr3:155464600-155487800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:155466400-155484600	Weak transcription	Fetal Brain Male	brain
13	chr3:155467000-155487200	Weak transcription	Fetal Brain Female	brain
14	chr3:155467200-155478400	Weak transcription	Fetal Intestine Large	intestine
15	chr3:155467200-155479400	Weak transcription	Fetal Intestine Small	intestine
16	chr3:155467200-155500200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:155467200-155508000	Weak transcription	K562	blood
18	chr3:155467200-155508800	Weak transcription	Hela-S3	cervix
19	chr3:155467400-155481600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:155467400-155508400	Weak transcription	HepG2	liver
21	chr3:155468000-155487200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr3:155469400-155481600	Weak transcription	Liver	Liver
23	chr3:155470000-155478800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr3:155470200-155483000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr3:155470400-155487400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr3:155470400-155487600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr3:155470800-155487400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr3:155471000-155481400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:155471000-155487400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:155471000-155487800	Weak transcription	Right Ventricle	heart
31	chr3:155471200-155487600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:155471400-155509000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr3:155471800-155487600	Weak transcription	Brain Angular Gyrus	brain
34	chr3:155472200-155487600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr3:155472400-155487200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:155472800-155488000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:155472800-155500000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:155473200-155487400	Weak transcription	Fetal Muscle Leg	muscle
39	chr3:155473200-155487400	Weak transcription	Thymus	Thymus
40	chr3:155474200-155487600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr3:155474200-155487800	Weak transcription	Spleen	Spleen
42	chr3:155474200-155490600	Weak transcription	Colon Smooth Muscle	Colon
43	chr3:155474200-155497600	Weak transcription	Fetal Muscle Trunk	muscle
44	chr3:155474400-155492000	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr3:155474800-155476600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr3:155474800-155487400	Weak transcription	Dnd41	blood
47	chr3:155474800-155487800	Weak transcription	Primary T cells from cord blood	blood
48	chr3:155474800-155489000	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr3:155475200-155491000	Weak transcription	Rectal Smooth Muscle	rectum
50	chr3:155475200-155492200	Weak transcription	Fetal Kidney	kidney

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