Variant report

Variant	esv3401275
Chromosome Location	chr2:9775301-9779799
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	ARID3A	chr2:9778752-9778986	K562	blood:	n/a	n/a
2	ARID3A	chr2:9777460-9777529	HepG2	liver:	n/a	n/a
3	ATF3	chr2:9778698-9778919	K562	blood:	n/a	n/a
4	BACH1	chr2:9778912-9779031	K562	blood:	n/a	n/a
5	BATF	chr2:9777365-9777778	GM12878	blood:	n/a	chr2:9777537-9777547 chr2:9777536-9777547
6	BHLHE40	chr2:9778643-9778972	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:9777509-9777817	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:9778655-9778966	A549	lung:	n/a	n/a
9	BHLHE40	chr2:9778575-9779051	K562	blood:	n/a	n/a
10	CBX3	chr2:9778593-9779038	K562	blood:	n/a	n/a
11	CCNT2	chr2:9778683-9778952	K562	blood:	n/a	n/a
12	CEBPB	chr2:9778803-9779007	K562	blood:	n/a	n/a
13	CHD2	chr2:9778686-9778935	Hela-S3	cervix:	n/a	n/a
14	CUX1	chr2:9778756-9779165	K562	blood:	n/a	n/a
15	CUX1	chr2:9777722-9777732	GM12878	blood:	n/a	n/a
16	EBF1	chr2:9777456-9777847	GM12878	blood:	n/a	n/a
17	EP300	chr2:9777468-9777743	GM12878	blood:	n/a	chr2:9777535-9777544 chr2:9777536-9777545
18	EP300	chr2:9778636-9778987	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr2:9778670-9779070	K562	blood:	n/a	n/a
20	EP300	chr2:9778763-9778958	K562	blood:	n/a	n/a
21	EP300	chr2:9778636-9778956	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr2:9777471-9777819	SK-N-SH_RA	brain:	n/a	chr2:9777535-9777544 chr2:9777536-9777545
23	EP300	chr2:9777436-9777758	SK-N-SH_RA	brain:	n/a	chr2:9777535-9777544 chr2:9777536-9777545
24	EP300	chr2:9777387-9777664	GM12878	blood:	n/a	chr2:9777535-9777544 chr2:9777536-9777545
25	EP300	chr2:9779168-9779525	SK-N-SH_RA	brain:	n/a	chr2:9779217-9779230
26	FOS	chr2:9777363-9777720	MCF10A-Er-Src	breast:	n/a	chr2:9777536-9777545 chr2:9777534-9777545 chr2:9777536-9777543 chr2:9777535-9777544 chr2:9777536-9777544
27	FOS	chr2:9778695-9779055	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr2:9777332-9777754	HUVEC	blood vessel:	n/a	chr2:9777536-9777545 chr2:9777534-9777545 chr2:9777536-9777543 chr2:9777535-9777544 chr2:9777536-9777544
29	FOS	chr2:9777398-9777688	MCF10A-Er-Src	breast:	n/a	chr2:9777536-9777545 chr2:9777534-9777545 chr2:9777536-9777543 chr2:9777535-9777544 chr2:9777536-9777544
30	FOS	chr2:9777368-9777720	MCF10A-Er-Src	breast:	n/a	chr2:9777536-9777545 chr2:9777534-9777545 chr2:9777536-9777543 chr2:9777535-9777544 chr2:9777536-9777544
31	FOS	chr2:9778679-9779008	HUVEC	blood vessel:	n/a	n/a
32	FOS	chr2:9778692-9778971	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr2:9778776-9778891	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr2:9777409-9777685	MCF10A-Er-Src	breast:	n/a	chr2:9777536-9777545 chr2:9777534-9777545 chr2:9777536-9777543 chr2:9777535-9777544 chr2:9777536-9777544
35	FOS	chr2:9778721-9778966	MCF10A-Er-Src	breast:	n/a	n/a
36	FOSL1	chr2:9777185-9777909	HCT-116	colon:	n/a	chr2:9777536-9777545 chr2:9777536-9777543 chr2:9777305-9777319 chr2:9777535-9777544 chr2:9777536-9777544
37	FOSL2	chr2:9778600-9779032	HepG2	liver:	n/a	n/a
38	FOSL2	chr2:9778579-9779478	A549	lung:	n/a	n/a
39	FOSL2	chr2:9777208-9777879	SK-N-SH	brain:	n/a	chr2:9777536-9777545 chr2:9777536-9777543 chr2:9777305-9777319 chr2:9777535-9777544 chr2:9777536-9777544
40	FOSL2	chr2:9778599-9778996	A549	lung:	n/a	n/a
41	FOSL2	chr2:9777248-9777830	A549	lung:	n/a	chr2:9777536-9777545 chr2:9777536-9777543 chr2:9777305-9777319 chr2:9777535-9777544 chr2:9777536-9777544
42	FOXA1	chr2:9778639-9778981	HepG2	liver:	n/a	n/a
43	FOXA2	chr2:9778513-9779077	A549	lung:	n/a	n/a
44	FOXP2	chr2:9778567-9778961	PFSK-1	brain:	n/a	n/a
45	GATA2	chr2:9777379-9777779	HUVEC	blood vessel:	n/a	n/a
46	GATA3	chr2:9775968-9776561	MCF-7	breast:	n/a	n/a
47	GATA3	chr2:9776092-9776375	MCF-7	breast:	n/a	n/a
48	GATA3	chr2:9777230-9778047	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr2:9777255-9777988	SK-N-SH	brain:	n/a	n/a
50	HCFC1	chr2:9778537-9778851	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9778686-9778736	HUVEC	blood vessel:	n/a
2	chr2:9778686-9778736	HUVEC	blood vessel:	n/a
3	chr2:9778686-9778736	HNPCEpiC	eye:	n/a
4	chr2:9778686-9778736	MCF-7	breast:	n/a
5	chr2:9778686-9778736	ECC-1	luminal epithelium:	n/a
6	chr2:9778686-9778736	U87	brain:	n/a
7	chr2:9778686-9778736	NB4	blood:	n/a
8	chr2:9778686-9778736	ovcar-3	ovarian:	n/a
9	chr2:9778686-9778736	HEEpiC	esophagus:	n/a
10	chr2:9778686-9778736	HRPEpiC	eye:	n/a
11	chr2:9778686-9778736	HepG2	liver:	n/a
12	chr2:9778686-9778736	NHDF-neo	bronchial:	n/a
13	chr2:9778686-9778736	HCPEpiC	choroid plexus:	n/a
14	chr2:9778686-9778736	HIPEpiC	eye:	n/a
15	chr2:9778686-9778736	SKMC	muscle:	n/a
16	chr2:9778686-9778736	HRE	kidney:	n/a
17	chr2:9778686-9778736	ProgFib	skin:	n/a
18	chr2:9778686-9778736	BJ	skin:	n/a
19	chr2:9778686-9778736	Hepatocyte	liver:	n/a
20	chr2:9778686-9778736	T-47D	breast:	n/a
21	chr2:9778686-9778736	NT2-D1	testis:	n/a
22	chr2:9778686-9778736	LNCaP	prostate:	n/a
23	chr2:9778686-9778736	SK-N-MC	brain:	n/a
24	chr2:9778686-9778736	SK-N-SH_RA	brain:	n/a
25	chr2:9778686-9778736	GM12891	blood:	n/a
26	chr2:9778686-9778736	H1-hESC	embryonic stem cell:	embryo
27	chr2:9778686-9778736	NH-A	brain:	n/a
28	chr2:9778686-9778736	IMR90	lung:	fetal
29	chr2:9778686-9778736	HCF	heart:	n/a
30	chr2:9778686-9778736	PANC-1	pancreas:	n/a
31	chr2:9778686-9778736	Hela-S3	cervix:	n/a
32	chr2:9778686-9778736	PFSK-1	brain:	n/a
33	chr2:9778686-9778736	HCM	heart:	n/a
34	chr2:9778686-9778736	GM19239	blood:	n/a
35	chr2:9778686-9778736	MCF10A-Er-Src	breast:	n/a
36	chr2:9778686-9778736	SK-N-SH	brain:	n/a
37	chr2:9778686-9778736	CMK	blood:	n/a
38	chr2:9778686-9778736	HMEC	breast:	n/a
39	chr2:9778686-9778736	HRCEpiC	kidney:	n/a
40	chr2:9778686-9778736	AG09319	gingival:	n/a
41	chr2:9778686-9778736	GM12878	blood:	n/a
42	chr2:9778686-9778736	AG04449	skin:	fetal
43	chr2:9778686-9778736	AoSMC	blood vessel:	n/a
44	chr2:9778686-9778736	K562	blood:	n/a
45	chr2:9778686-9778736	SAEC	small airway:	n/a
46	chr2:9778686-9778736	HEK293	kidney:	embryo
47	chr2:9778686-9778736	GM06990	blood:	n/a
48	chr2:9778686-9778736	HAEpiC	amniotic membrane:	n/a
49	chr2:9778686-9778736	RPTEC	kidney:	n/a
50	chr2:9778686-9778736	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:9695463..9697852-chr2:9775968..9778612,3	K562	blood:
2	chr2:9779400..9780949-chr2:9782818..9785036,2	K562	blood:
3	chr2:9695095..9696650-chr2:9774545..9776694,2	MCF-7	breast:
4	chr2:9774003..9777519-chr2:9779253..9781345,3	MCF-7	breast:
5	chr2:9777094..9779295-chr2:10091033..10093180,2	MCF-7	breast:
6	chr2:9774726..9777001-chr2:9783752..9786208,2	MCF-7	breast:
7	chr2:9767473..9774138-chr2:9774735..9780659,16	MCF-7	breast:
8	chr2:9695463..9697852-chr2:9776763..9778612,2	K562	blood:
9	chr2:9769155..9773590-chr2:9774278..9779571,11	MCF-7	breast:
10	chr2:9775999..9777968-chr2:9781245..9783504,2	K562	blood:
11	chr2:9776400..9778601-chr2:9910278..9912270,2	K562	blood:
12	chr2:9774003..9777519-chr2:9779253..9781345,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IAH1-3	chr2:9778900-9779050	NONHSAT069062
2	lnc-IAH1-3	chr2:9778901-9779050	XLOC_001339

Variant related genes	Relation type
ENSG00000240687	TF binding region
YWHAQ	TF binding region
ENSG00000240687	CpG island
YWHAQ	CpG island
ENSG00000151694	chromatin interactions
ENSG00000134317	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000243491	chromatin interactions
ENSG00000134308	chromatin interactions

Extended variants
information (count: 167 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:167 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116800664	chr2:9775314-9775315	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs139613814	chr2:9775329-9775330	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145242168	chr2:9775333-9775334	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs114255267	chr2:9775388-9775389	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs536929858	chr2:9775401-9775402	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs546740159	chr2:9775444-9775445	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs186045212	chr2:9775475-9775476	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147210542	chr2:9775514-9775515	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs545229414	chr2:9775523-9775524	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559198295	chr2:9775537-9775538	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs572568006	chr2:9775580-9775581	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs114808126	chr2:9775587-9775588	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs75554208	chr2:9775615-9775616	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs62121162	chr2:9775619-9775620	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs566225228	chr2:9775621-9775622	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs561248498	chr2:9775632-9775633	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs538850218	chr2:9775638-9775639	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs75865312	chr2:9775654-9775655	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs530143002	chr2:9775655-9775656	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs62121163	chr2:9775657-9775658	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs140635891	chr2:9775663-9775664	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs199693838	chr2:9775691-9775692	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs190379990	chr2:9775706-9775707	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs535353895	chr2:9775729-9775730	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs377606257	chr2:9775730-9775731	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs80152469	chr2:9775737-9775738	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs532043134	chr2:9775774-9775775	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs370476459	chr2:9775786-9775787	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs182593247	chr2:9775819-9775820	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs547909932	chr2:9775853-9775854	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs567837862	chr2:9775859-9775860	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs536609435	chr2:9775902-9775903	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs556927895	chr2:9775917-9775918	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs570205919	chr2:9775960-9775961	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs116053977	chr2:9775966-9775967	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs564627602	chr2:9775972-9775973	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs34084070	chr2:9776015-9776016	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs113765682	chr2:9776043-9776044	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs148939843	chr2:9776077-9776078	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs142870125	chr2:9776078-9776079	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs537451870	chr2:9776087-9776088	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs555069362	chr2:9776101-9776102	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs551969042	chr2:9776163-9776164	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs543409358	chr2:9776183-9776184	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs151064034	chr2:9776195-9776196	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs187059861	chr2:9776200-9776201	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs546116195	chr2:9776222-9776223	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs559102979	chr2:9776229-9776230	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs377340166	chr2:9776261-9776262	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs6723929	chr2:9776291-9776292	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9771600-9777800	Weak transcription	Lung	lung
2	chr2:9772000-9777800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:9772000-9778400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:9772200-9776600	Weak transcription	Brain Angular Gyrus	brain
5	chr2:9772200-9777000	Weak transcription	K562	blood
6	chr2:9772200-9777200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:9772200-9781800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:9772400-9776200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:9772400-9776200	Weak transcription	Brain Anterior Caudate	brain
10	chr2:9772400-9776400	Weak transcription	HMEC	breast
11	chr2:9772400-9777000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:9772400-9777200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr2:9772400-9777600	Weak transcription	Hela-S3	cervix
14	chr2:9772400-9778000	Weak transcription	Right Atrium	heart
15	chr2:9772600-9776200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr2:9772600-9776400	Weak transcription	Brain Substantia Nigra	brain
17	chr2:9772600-9776800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:9772600-9777000	Weak transcription	NH-A	brain
19	chr2:9772600-9777600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:9772600-9777800	Weak transcription	Left Ventricle	heart
21	chr2:9772800-9777000	Weak transcription	NHEK	skin
22	chr2:9772800-9777200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:9772800-9777600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:9772800-9780200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr2:9773000-9776200	Weak transcription	Brain Hippocampus Middle	brain
26	chr2:9773000-9776600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:9773000-9776800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:9773000-9776800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:9773000-9777000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:9773000-9777000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:9773000-9777600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:9773000-9777600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:9773000-9778200	Weak transcription	Right Ventricle	heart
34	chr2:9773000-9778400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:9773000-9778400	Weak transcription	Fetal Intestine Small	intestine
36	chr2:9773200-9776400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr2:9773200-9776800	Weak transcription	NHLF	lung
38	chr2:9773200-9776800	Weak transcription	Osteobl	bone
39	chr2:9773400-9777000	Weak transcription	HSMMtube	muscle
40	chr2:9773400-9777600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:9773600-9776600	Weak transcription	HSMM	muscle
42	chr2:9773600-9776600	Weak transcription	NHDF-Ad	bronchial
43	chr2:9773600-9776800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:9773600-9776800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:9773600-9777000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:9773600-9777000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr2:9773600-9777400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:9773600-9777600	Weak transcription	Fetal Muscle Trunk	muscle
49	chr2:9773600-9777800	Weak transcription	Placenta	Placenta
50	chr2:9773600-9778000	Weak transcription	Psoas Muscle	Psoas

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