Variant report

Variant	nsv2967
Chromosome Location	chr2:151026829-151039101
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	ATF1	chr2:151028405-151028790	K562	blood:	n/a	n/a
2	ATF1	chr2:151035039-151035302	K562	blood:	n/a	n/a
3	CEBPB	chr2:151034990-151035488	MCF-7	breast:	n/a	n/a
4	CEBPB	chr2:151035071-151035430	MCF-7	breast:	n/a	n/a
5	CEBPB	chr2:151035131-151035201	A549	lung:	n/a	n/a
6	CEBPB	chr2:151034980-151035502	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:151034966-151035444	A549	lung:	n/a	n/a
8	CTCF	chr2:151028080-151028230	GM12870	blood:	n/a	n/a
9	CTCF	chr2:151027528-151027589	GM20000	blood:	n/a	n/a
10	CTCF	chr2:151030313-151030354	Kidney_OC	kidney:	n/a	n/a
11	EP300	chr2:151035040-151035568	T-47D	breast:	n/a	n/a
12	EP300	chr2:151039020-151039654	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr2:151038787-151039964	SK-N-SH	brain:	n/a	n/a
14	EP300	chr2:151035080-151035432	Hela-S3	cervix:	n/a	n/a
15	EP300	chr2:151038993-151039772	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr2:151038875-151039597	ECC-1	luminal epithelium:	n/a	n/a
17	FOS	chr2:151030528-151031038	HUVEC	blood vessel:	n/a	chr2:151030565-151030572 chr2:151030895-151030907
18	FOS	chr2:151035722-151035760	MCF10A-Er-Src	breast:	n/a	chr2:151035743-151035752 chr2:151035745-151035752
19	FOXA1	chr2:151030885-151031224	T-47D	breast:	n/a	chr2:151031141-151031153 chr2:151031139-151031154
20	FOXA1	chr2:151035106-151035483	T-47D	breast:	n/a	n/a
21	FOXA1	chr2:151035102-151035559	T-47D	breast:	n/a	n/a
22	FOXA2	chr2:151030914-151031490	A549	lung:	n/a	chr2:151031141-151031153
23	GATA2	chr2:151038845-151039702	SH-SY5Y	brain:	n/a	chr2:151039318-151039329 chr2:151039568-151039577 chr2:151039655-151039662
24	GATA3	chr2:151038856-151039562	A549	lung:	n/a	chr2:151039318-151039329
25	GATA3	chr2:151038941-151039559	A549	lung:	n/a	chr2:151039318-151039329
26	GATA3	chr2:151035190-151035546	MCF-7	breast:	n/a	n/a
27	GATA3	chr2:151038888-151039814	SK-N-SH	brain:	n/a	chr2:151039318-151039329 chr2:151039568-151039577 chr2:151039655-151039662
28	GATA3	chr2:151038962-151039848	SK-N-SH	brain:	n/a	chr2:151039318-151039329 chr2:151039568-151039577 chr2:151039655-151039662
29	GATA3	chr2:151034944-151035725	MCF-7	breast:	n/a	chr2:151035639-151035646
30	GATA3	chr2:151035105-151035440	MCF-7	breast:	n/a	n/a
31	GATA3	chr2:151029599-151029802	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr2:151038911-151039474	MCF-7	breast:	n/a	chr2:151039318-151039329
33	GATA3	chr2:151034963-151035828	MCF-7	breast:	n/a	chr2:151035639-151035646
34	GATA3	chr2:151035027-151035586	T-47D	breast:	n/a	n/a
35	GATA3	chr2:151038893-151039810	SH-SY5Y	brain:	n/a	chr2:151039318-151039329 chr2:151039568-151039577 chr2:151039655-151039662
36	GATA3	chr2:151035143-151035563	A549	lung:	n/a	n/a
37	GATA3	chr2:151035049-151035562	T-47D	breast:	n/a	n/a
38	GATA3	chr2:151035428-151035494	SH-SY5Y	brain:	n/a	n/a
39	IRF1	chr2:151030806-151030930	K562	blood:	n/a	n/a
40	JUN	chr2:151035626-151035737	HepG2	liver:	n/a	n/a
41	JUN	chr2:151035659-151035834	K562	blood:	n/a	chr2:151035743-151035752 chr2:151035745-151035752
42	JUND	chr2:151030071-151030179	K562	blood:	n/a	n/a
43	JUND	chr2:151035398-151035452	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr2:151035014-151035660	T-47D	breast:	n/a	n/a
45	JUND	chr2:151035610-151035810	K562	blood:	n/a	chr2:151035742-151035753 chr2:151035743-151035752 chr2:151035745-151035752
46	JUND	chr2:151035621-151035835	HepG2	liver:	n/a	chr2:151035742-151035753 chr2:151035743-151035752 chr2:151035745-151035752
47	JUND	chr2:151035136-151035538	T-47D	breast:	n/a	n/a
48	MAX	chr2:151035543-151035756	K562	blood:	n/a	n/a
49	MAX	chr2:151035482-151035795	MCF-7	breast:	n/a	n/a
50	MAX	chr2:151027750-151028043	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:151027710-151027760	GM12891	blood:	n/a
2	chr2:151027710-151027760	Hepatocyte	liver:	n/a
3	chr2:151027710-151027760	SK-N-MC	brain:	n/a
4	chr2:151027710-151027760	HCT-116	colon:	n/a
5	chr2:151027710-151027760	AG04449	skin:	fetal
6	chr2:151027710-151027760	NT2-D1	testis:	n/a
7	chr2:151027710-151027760	HCM	heart:	n/a
8	chr2:151027710-151027760	HRCEpiC	kidney:	n/a
9	chr2:151027710-151027760	GM19239	blood:	n/a
10	chr2:151027710-151027760	Caco-2	colon:	n/a
11	chr2:151027710-151027760	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:151027710-151027760	AoSMC	blood vessel:	n/a
13	chr2:151027710-151027760	Jurkat	blood:	n/a
14	chr2:151027710-151027760	PrEC	prostate:	n/a
15	chr2:151027710-151027760	U87	brain:	n/a
16	chr2:151027710-151027760	GM12878	blood:	n/a
17	chr2:151027710-151027760	SAEC	small airway:	n/a
18	chr2:151027710-151027760	SKMC	muscle:	n/a
19	chr2:151027710-151027760	BJ	skin:	n/a
20	chr2:151027710-151027760	SK-N-SH	brain:	n/a
21	chr2:151027710-151027760	AG09309	skin:	n/a
22	chr2:151027710-151027760	HepG2	liver:	n/a
23	chr2:151027710-151027760	AG09319	gingival:	n/a
24	chr2:151027710-151027760	MCF-7	breast:	n/a
25	chr2:151027710-151027760	HUVEC	blood vessel:	n/a
26	chr2:151027710-151027760	T-47D	breast:	n/a
27	chr2:151027710-151027760	ProgFib	skin:	n/a
28	chr2:151027710-151027760	NH-A	brain:	n/a
29	chr2:151027710-151027760	NHDF-neo	bronchial:	n/a
30	chr2:151027710-151027760	MCF10A-Er-Src	breast:	n/a
31	chr2:151027710-151027760	HRE	kidney:	n/a
32	chr2:151027710-151027760	PFSK-1	brain:	n/a
33	chr2:151027710-151027760	HEEpiC	esophagus:	n/a
34	chr2:151027710-151027760	ovcar-3	ovarian:	n/a
35	chr2:151027710-151027760	AG04450	lung:	fetal
36	chr2:151027710-151027760	Hela-S3	cervix:	n/a
37	chr2:151027710-151027760	LNCaP	prostate:	n/a
38	chr2:151027710-151027760	BE2_C	brain:	n/a
39	chr2:151027710-151027760	HEK293	kidney:	embryo
40	chr2:151027710-151027760	ECC-1	luminal epithelium:	n/a
41	chr2:151027710-151027760	AG10803	skin:	n/a
42	chr2:151027710-151027760	RPTEC	kidney:	n/a
43	chr2:151027710-151027760	H1-hESC	embryonic stem cell:	embryo
44	chr2:151027710-151027760	HCF	heart:	n/a
45	chr2:151027710-151027760	HNPCEpiC	eye:	n/a
46	chr2:151027710-151027760	GM06990	blood:	n/a
47	chr2:151027710-151027760	HMEC	breast:	n/a
48	chr2:151027710-151027760	CMK	blood:	n/a
49	chr2:151027710-151027760	HAEpiC	amniotic membrane:	n/a
50	chr2:151027710-151027760	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:151025085..151027146-chr2:151027265..151029673,2	MCF-7	breast:
2	chr2:151024105..151026870-chr2:151120233..151122729,2	MCF-7	breast:
3	chr2:151015327..151017230-chr2:151030179..151032620,2	K562	blood:

Variant related genes	Relation type
ENSG00000230645	TF binding region
ENSG00000230645	CpG island
ENSG00000230645	chromatin interactions

Extended variants
information (count: 455 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6707784	chr2:151026829-151026830	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140108678	chr2:151026842-151026843	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572532540	chr2:151026845-151026846	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142466715	chr2:151026854-151026855	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151319045	chr2:151026875-151026876	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6721152	chr2:151026877-151026878	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs116548406	chr2:151026878-151026879	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372400103	chr2:151026894-151026895	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191754979	chr2:151026932-151026933	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139269650	chr2:151026943-151026944	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531569920	chr2:151026969-151026970	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147704916	chr2:151026983-151026984	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76741733	chr2:151026993-151026994	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181551550	chr2:151027012-151027013	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76816801	chr2:151027020-151027021	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142432674	chr2:151027029-151027030	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569643749	chr2:151027049-151027050	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535385750	chr2:151027070-151027071	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs555341688	chr2:151027075-151027076	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566076595	chr2:151027081-151027082	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146466441	chr2:151027090-151027091	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558270045	chr2:151027134-151027135	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6750791	chr2:151027141-151027142	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565197279	chr2:151027142-151027143	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147616983	chr2:151027144-151027145	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114398884	chr2:151027151-151027152	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs117730961	chr2:151027158-151027159	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs114838980	chr2:151027185-151027186	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs6708312	chr2:151027186-151027187	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs111954774	chr2:151027187-151027188	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs185574112	chr2:151027189-151027190	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs142131385	chr2:151027190-151027191	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs114144810	chr2:151027197-151027198	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs143196461	chr2:151027203-151027204	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs549264297	chr2:151027210-151027211	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111606371	chr2:151027216-151027217	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs535050230	chr2:151027223-151027224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557842295	chr2:151027245-151027246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575099873	chr2:151027251-151027252	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571637448	chr2:151027305-151027306	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs537558000	chr2:151027307-151027308	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557450714	chr2:151027386-151027387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs574286753	chr2:151027401-151027402	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs542848971	chr2:151027404-151027405	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548270386	chr2:151027405-151027406	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs148266830	chr2:151027423-151027424	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs541049756	chr2:151027487-151027488	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs141168817	chr2:151027490-151027491	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs577185834	chr2:151027495-151027496	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373823094	chr2:151027505-151027506	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151025400-151030600	Weak transcription	HUVEC	blood vessel
2	chr2:151026000-151027200	Flanking Active TSS	Liver	Liver
3	chr2:151026000-151027400	Enhancers	Dnd41	blood
4	chr2:151026400-151028600	Weak transcription	A549	lung
5	chr2:151026400-151030600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:151026400-151030600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:151026600-151031200	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:151026800-151030600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:151026800-151030600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:151027200-151029400	Weak transcription	Liver	Liver
11	chr2:151028400-151028600	Enhancers	Fetal Kidney	kidney
12	chr2:151028600-151028800	Enhancers	A549	lung
13	chr2:151028600-151030600	Weak transcription	Fetal Kidney	kidney
14	chr2:151028800-151029200	Weak transcription	A549	lung
15	chr2:151029200-151031400	Enhancers	A549	lung
16	chr2:151029400-151031400	Enhancers	Liver	Liver
17	chr2:151030600-151030800	Enhancers	HSMMtube	muscle
18	chr2:151030600-151031000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:151030600-151031000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:151030600-151031400	Enhancers	Fetal Kidney	kidney
21	chr2:151030600-151031400	Enhancers	HUVEC	blood vessel
22	chr2:151030600-151031800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:151030600-151032000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:151030600-151032200	Enhancers	Fetal Lung	lung
25	chr2:151030800-151031200	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr2:151030800-151032200	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr2:151030800-151032400	Enhancers	Fetal Intestine Large	intestine
28	chr2:151031200-151031600	Enhancers	Colon Smooth Muscle	Colon
29	chr2:151031200-151031600	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr2:151031400-151031800	Flanking Active TSS	Liver	Liver
31	chr2:151031400-151031800	Weak transcription	Fetal Kidney	kidney
32	chr2:151031400-151031800	Flanking Active TSS	A549	lung
33	chr2:151031600-151031800	Enhancers	HSMMtube	muscle
34	chr2:151031600-151032000	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr2:151031600-151032000	Enhancers	HSMM	muscle
36	chr2:151031600-151034800	Weak transcription	Colon Smooth Muscle	Colon
37	chr2:151031800-151032000	Enhancers	Fetal Kidney	kidney
38	chr2:151031800-151032000	Enhancers	A549	lung
39	chr2:151031800-151032200	Enhancers	Liver	Liver
40	chr2:151031800-151032200	Enhancers	Duodenum Mucosa	Duodenum
41	chr2:151031800-151032200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr2:151031800-151032200	Enhancers	Fetal Intestine Small	intestine
43	chr2:151032000-151033200	Weak transcription	Fetal Kidney	kidney
44	chr2:151032000-151034800	Weak transcription	A549	lung
45	chr2:151032000-151035000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr2:151032200-151033000	Weak transcription	Fetal Intestine Small	intestine
47	chr2:151032200-151033200	Weak transcription	Liver	Liver
48	chr2:151032200-151035200	Weak transcription	Fetal Lung	lung
49	chr2:151032200-151035400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr2:151032400-151032800	Weak transcription	Fetal Intestine Large	intestine

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